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Which rules apply to cheese?

We track 7,263 rules for these in 19 of 21 markets, including California's Prop 65 list of 883 chemicals. Check your product free, no account needed.

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Packaged food and beverages / Dairy and plant-based alternatives / Cheese

Natural and processed cheese (listeria criteria in EU 2073/2005, not covered here).

Food: partial coverage. Food verdicts cover labelling and import duties. Additive and contaminant limits are not yet in the rule data, so a food result is not a full check of what the product may contain.

Rules

Rules by market

Open a market to read its rules for this category.

United States (federal)640 rulesCoverage: Main sources, from 7 Oct 2026
Main sources, from 7 Oct 2026 · What is covered

Federal food regulations as published on 7 Oct 2026.

United States (federal): main sources stored. Modelled: TSCA section 8(a)(7) PFAS reporting and recordkeeping (40 CFR 705), shown as applying only if the product contains a PFAS; 21 CFR 101 food labelling (statement of identity, net quantity, ingredient list, allergen declaration incl. sesame under FALCPA and FASTER, nutrition facts, name and place of business); FD&C Act sec. 403 misbranding (21 U.S.C. 343); 21 CFR 170-189 additive status where listable (172 direct additives, 173, 180, 182 GRAS substances, 184); facility registration (21 CFR 1 subpart H); prior notice (subpart I); FSMA FSVP (21 CFR 1 subpart L). Not stored: GRAS notices outside the listed 21 CFR parts; standards of identity (21 CFR 130-169); Part 117 preventive-control details (only who must comply and the qualified-facility rules are encoded); seafood and juice HACCP; FPLA and 16 CFR 500; FDA action levels and guidance levels for contaminants (not binding limits); state laws other than listed; USDA-regulated meat; poultry and egg products; dietary supplements; infant formula.

Requirement
Applies when
Effective
Source
Notification
PFAS as defined in United States (federal)

Notification to US EPA through the Central Data Exchange (CDX), the PFAS 8(a)(7) reporting tool (§705.35)

Submit the §705.15 information (or, for article importers, the §705.18(a) streamlined form) during the submission period. §705.20(a): the submission period begins January 31, 2027, or 60 days following the date EPA announces in the Federal Register under paragraph (c), whichever is earlier, and lasts six months. §705.20(b): a small manufacturer (40 CFR 704.3) reporting exclusively as an article importer under §705.18(a) has twelve months from the same start. §705.25: keep the records that document what was reported for 5 years beginning on the last day of the submission period.

Exemptions (2)

Reporting is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste

“Reporting under this part is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste.”
§705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

Reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage

“Additionally, reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage.”
§705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
Later deadlines (1)

31 Jan 2027: Submission period starts on this date at the latest (earlier if EPA announces a date: 60 days after it); it lasts six months, or twelve months for a small manufacturer reporting only as an article importer

“the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier, and last for six months.”
§705.20(a) (excerpt) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
Penalty

Failure or refusal to submit the information, or to keep and give access to the records, is unlawful under TSCA section 15(3); a person who violates TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted (no penalty amount is stated in this part)

“TSCA section 16 provides that any person who violates a provision of TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted.”
§705.1(b) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 22 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-22 per the eCFR (title 40 up to date as of 2026-10-22). Section 705.20 carries the amendment 91 FR 18789, Apr. 13, 2026.

  • Your role: Manufacturer or Importer
  • You manufactured (including imported) a PFAS, or an article containing one, for commercial purposes at any time from January 1, 2011 through December 31, 2022

Depends on: economic operator role

Takes effect 31 Jan 2027

Applies to products manufactured on or after 31 Jan 2027

Stated in §705.20(a)-(b): “the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier”. Paragraph (c): “EPA intends to publish a document in the Federal Register announcing the submission period date and revising or removing this paragraph (c).” The period had not begun on the date this row was made (2026-10-26); the date is the latest start the text allows.

“All information reported to EPA in response to the requirements of this part must be submitted during the applicable submission period.”
§705.20(a) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

Every product in the category

Dates run from 15 Mar 1977 to 7 Sep 2005

Each rule has its own date; open a target.

Example: Calamus and its derivatives

“§ 189.110 Calamus and its derivatives. (a) Calamus is the dried rhizome of Acorus calamus L. It has been used as a flavoring compound, especially as the oil or extract.”
Parts 172-189 substance sections, 21 CFR 189.110, Subpart Substances Generally Prohibited From Direct Addition or Use as Human Food · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
Ban
Flectol H

Banned

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • It contains Flectol H

In force since 15 Mar 1977

Applies to products sold on or after 15 Mar 1977

Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

“§ 189.220 Flectol H. (a) Flectol H is the chemical 1,2-dihydro-2,2,4-trimethylquinoline, polymerized, C12H15N. It is a synthetic chemical not found in natural products, and has been used as a component of food packaging adhesives.”
Parts 172-189 substance sections, 21 CFR 189.220, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
Ban
Mercaptoimidazoline and 2-mercaptoimidazoline

Banned

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • It contains mercaptoimidazoline or 2-mercaptoimidazoline

In force since 15 Mar 1977

Applies to products sold on or after 15 Mar 1977

Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

“§ 189.250 Mercaptoimidazoline and 2-mercaptoimidazoline. (a) Mercaptoimidazoline and 2-mercaptoimidazoline both have the molecular formula C3H6N2S. They are synthetic chemicals not found in natural products and have been used in the production of rubber articles that may come into contact with food.”
Parts 172-189 substance sections, 21 CFR 189.250, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
Ban
4,4′-Methylenebis (2-chloroanaline)

Banned

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • It contains 4,4′-methylenebis (2-chloroanaline)

In force since 15 Mar 1977

Applies to products sold on or after 15 Mar 1977

Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

“§ 189.280 4,4′-Methylenebis (2-chloroanaline). (a) 4,4′-Methylenebis (2-chloroanaline) has the molecular formula, C13H12Cl2N2. It is a synthetic chemical not found in natural products and has been used as a polyurethane curing agent and as a component of food packaging adhesives and polyurethane resins.”
Parts 172-189 substance sections, 21 CFR 189.280, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
Ban
Hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins

Banned

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • It contains hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins

In force since 17 Feb 1989

Applies to products sold on or after 17 Feb 1989

Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

“§ 189.300 Hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins. (a) Hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins are the condensation product of 1 mole of triphenyl phosphite and 1.5 moles of hydrogenated 4,4′-isopropylidene-diphenol such that the finished resins have a molecular weight in the range of 2,400 to 3,000. They are synthetic chemicals not found in natural products and have been used as antioxidants and as stabilizers in vinyl chloride polymer resins when such polymer resins are used in the manufacture of rigid vinyl chloride polymer bottles.”
Parts 172-189 substance sections, 21 CFR 189.300, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
Ban

If it is offered for sale under the name of another food.

Banned

The start date is not stated in the text (date unknown).

Official text, current to 31 Dec 2024. United States Code, 2024 Edition, published by GPO; amendments enacted after the edition are not in this text.

Every product in the category

In force, start date unknown

In force no later than 2024-01-01 (the stored 2024 edition's date); earlier commencement is not stated in the published text.

“If it is offered for sale under the name of another food.”
343(b) · fetched 2026-10-09US Government Publishing Office (GovInfo, USCODE-2024 edition): 21 U.S.C. 343 (2024 Edition)(opens in a new tab)
Notification
PFAS as defined in United States (federal)

Notification to US EPA through the Central Data Exchange (CDX), the PFAS 8(a)(7) reporting tool (§705.35)

Persons who manufactured a PFAS, including as an importer, for commercial purposes at any period from January 1, 2011 through the end of the last calendar year before November 13, 2023 must report to EPA. §705.1(a): “This part specifies reporting and recordkeeping procedures for manufacturers (including importers) of per- and polyfluoroalkyl substances (hereafter referred to as PFAS) under section 8(a)(7) of the Toxic Substances Control Act (TSCA).” §705.5: “The requirements of this part apply to all chemical substances and mixtures containing a chemical substance (including articles) that are a PFAS, consistent with the definition of PFAS at § 705.3.” §705.18(a): an importer of an article that contains a PFAS may use a streamlined article-importer form for each year since January 1, 2011 in which the PFAS was imported in an article. PFAS is defined in §705.3 by three structural sub-structures; this check lists the rule for a product only if it contains a PFAS.

Exemptions (2)

Reporting is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste

“Reporting under this part is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste.”
§705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

Reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage

“Additionally, reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage.”
§705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

The start date is not stated in the text (date unknown).

Penalty

Failure or refusal to submit the information, or to keep and give access to the records, is unlawful under TSCA section 15(3); a person who violates TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted (no penalty amount is stated in this part)

“TSCA section 16 provides that any person who violates a provision of TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted.”
§705.1(b) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 22 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-22 per the eCFR (title 40 up to date as of 2026-10-22). Section 705.20 carries the amendment 91 FR 18789, Apr. 13, 2026.

  • Your role: Manufacturer or Importer
  • You manufactured (including imported) a PFAS, or an article containing one, for commercial purposes at any time from January 1, 2011 through December 31, 2022

Depends on: economic operator role

In force, start date unknown

The text names November 13, 2023 only as the end of the look-back window in §705.10 (“the last calendar year prior to November 13, 2023”); it states no operative date of its own, so that date stands in. The one-time report covers each year since January 1, 2011; when it is due is in the §705.20 row.

“Persons who have manufactured for commercial purposes a chemical substance identified in § 705.5 at any period from January 1, 2011, through the end of the last calendar year prior to November 13, 2023, except as described in § 705.12, is subject to the requirements of this part.”
§705.10 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
Conformity

A claim that the product or its package is free of BPA or does not contain or use BPA.

Must meet the conditions of A claim that the product is free of BPA must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if BPA has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: BPA-free

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
§260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
Conformity

A compostable claim made for the product or its package.

Must meet the conditions of Do not misrepresent, directly or by implication, that the product or package is compostable.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: compostable

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product or package is compostable.”
§260.7(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.7(opens in a new tab)
Conformity

A degradable or biodegradable claim (including oxo-degradable, oxo-biodegradable and photodegradable claims) made for the product or its package.

Must meet the conditions of Do not misrepresent, directly or by implication, that the product or package is degradable, biodegradable, oxo-degradable, oxo-biodegradable or photodegradable.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: biodegradable

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product or package is degradable, biodegradable, oxo-degradable, oxo-biodegradable, or photodegradable.”
§260.8(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.8(opens in a new tab)
Conformity

A claim that the product or its package is free of formaldehyde or does not contain or use formaldehyde.

Must meet the conditions of A claim that the product is free of formaldehyde must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if formaldehyde has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: formaldehyde-free

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
§260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
Conformity

A general environmental benefit claim (for example "eco-friendly" or "green") made for the product or its package.

Must meet the conditions of Do not misrepresent, directly or by implication, that the product, package or service offers a general environmental benefit.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: eco-friendly

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product, package, or service offers a general environmental benefit.”
§260.4(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.4(opens in a new tab)
Conformity

A claim that the product or its package is free of lead or does not contain or use lead.

Must meet the conditions of A claim that the product is free of lead must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if lead has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: lead-free

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
§260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
Conformity

A non-toxic claim made for the product or its package.

Must meet the conditions of Do not misrepresent, directly or by implication, that the product, package or service is non-toxic. Qualify a non-toxic claim clearly and prominently to the extent necessary to avoid deception.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: non-toxic

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product, package, or service is non-toxic. Non-toxic claims should be clearly and prominently qualified to the extent necessary to avoid deception.”
§260.10(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.10(opens in a new tab)
Conformity

A claim that the product or its package is free of PFAS or does not contain or use PFAS.

Must meet the conditions of A claim that the product is free of PFAS must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if PFAS has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: PFAS-free

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
§260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
Conformity

A claim that the product or its package is free of PTFE or does not contain or use PTFE.

Must meet the conditions of A claim that the product is free of PTFE must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if PTFE has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: PTFE-free

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
§260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
Conformity

A recyclable claim made for the product or its package.

Must meet the conditions of Market the item as recyclable only if it can be collected, separated or otherwise recovered from the waste stream through an established recycling program for reuse or for use in making another item. Make an unqualified claim only when recycling facilities are available to a substantial majority (at least 60 percent) of consumers or communities where the item is sold; otherwise qualify the claim. Qualify which portions are recyclable when only some components are, and do not call the item recyclable if any component, or its shape or size, significantly limits recycling. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: recyclable

In force, start date unknown

The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

“A product or package should not be marketed as recyclable unless it can be collected, separated, or otherwise recovered from the waste stream through an established recycling program”
§260.12(a) (excerpt) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.12(opens in a new tab)
Conformity

A label that represents the product as Made in the United States without qualification.

Must meet the conditions of Label a product as Made in the United States only if its final assembly or processing occurs in the United States, all significant processing that goes into it occurs in the United States, and all or virtually all of its ingredients or components are made and sourced in the United States. The same applies to a seal, mark, tag or stamp in a mail order catalog or mail order promotional material. A violation is treated as a violation of a trade regulation rule under section 18 of the FTC Act.

The start date is not stated in the text (date unknown).

Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

  • Claim: Made in USA

In force, start date unknown

The text states only the Federal Register publication date of the rule (July 14, 2021); it states no separate effective date.

“all significant processing that goes into the product occurs in the United States, and all or virtually all ingredients or components of the product are made and sourced in the United States.”
§323.2 (excerpt) · fetched 2026-10-22US FTC via eCFR: 16 CFR 323.2(opens in a new tab)
Disclosure

If you give a written warranty, put all its terms in one clear document: who and what is covered, what you will do, how long, how to claim, and the required State-rights statements

Disclosure to buyer

Written warranty terms (16 CFR 701.3(a)): a warrantor who gives a written warranty on a consumer product costing the consumer more than $15.00 must clearly and conspicuously disclose, in a single document in simple and readily understood language: (1) who the warranty is extended to, if limited to the original purchaser or otherwise; (2) the products, parts or components covered and, where needed, excluded; (3) what the warrantor will do on a defect or failure, and what it will pay for or provide; (4) when the term starts if not on the purchase date, and how long it lasts; (5) step by step how to claim, with the warrantor's name and mailing address or responsible department, or a free telephone number; (6) any informal dispute settlement mechanism (part 703); (7) any limit on the duration of implied warranties, with "Some States do not allow limitations on how long an implied warranty lasts, so the above limitation may not apply to you."; (8) any exclusion or limit on incidental or consequential damages, with its State-law statement; (9) "This warranty gives you specific legal rights, and you may also have other rights which vary from State to State." If return of a registration card is a condition of coverage, the warranty must say so (701.4).

Exemptions (2)

Products bought solely for commercial or industrial use are excluded from this part; warranties that cover only a repairer's workmanship (services) are not covered by the Act (700.1(h)).

“Products which are purchased solely for commercial or industrial use are excluded solely for purposes of this part.”
16 CFR 701.1(b) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

Third-party emblems, seals or insignias promising replacement or refund, with no representation of quality or performance, are exempt from (a)(1)-(9) if the third party publishes the disclosures in each issue of a general-circulation publication and gives them free on written request.

“Paragraphs (a) (1) through (9) of this section shall not be applicable with respect to statements of general policy on emblems, seals or insignias issued by third parties promising replacement or refund if a consumer product is defective”
16 CFR 701.3(b) (excerpt) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 23 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; versioner date 2026-10-23.

  • It is a consumer product (tangible personal property normally used for personal, family or household purposes) (16 CFR 701.1(b), 702.1(b))
  • You give a written warranty on a consumer product that costs the consumer more than $15 (16 CFR 701.2: the rules apply to "written warranties on consumer products actually costing the consumer more than $15.00"; 701.1(h): a warrantor is "any supplier, manufacturer, or other person who gives or offers to give a written warranty")

In force since 1 Jan 1977

Applies to products manufactured on or after 1 Jan 1977

Parts 701 and 702 apply only to written warranties on products manufactured after December 31, 1976 (16 CFR 700.12); 702.3 was last revised at 81 FR 63669, Sept. 15, 2016 (online warranty terms option).

“Any warrantor warranting to a consumer by means of a written warranty a consumer product actually costing the consumer more than $15.00 shall clearly and conspicuously disclose in a single document in simple and readily understood language, the following items of information:”
16 CFR 701.3(a) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)
Disclosure

Make the written warranty's text available to the buyer before the sale (in store, catalog or online listing, door to door); the warrantor supplies the text or posts it online

Disclosure to buyer

Pre-sale availability of written warranty terms (16 CFR 702.3), for consumer products costing the consumer more than $15.00. Seller (702.3(a)): make the warranty text readily available before sale by displaying it close to the product, or by furnishing it on request with signs telling buyers it is available. Catalog and mail order sellers, including any offer whose ordering does not need a visit to the seller (702.3(c)): give the full text, or the warrantor's web address plus where to request a free copy, beside the product description or in a referenced section. Door-to-door sellers: say before the sale that the warranties may be inspected (702.3(d)). Warrantor (702.3(b)(1)): give sellers the warranty materials (a copy with every product, a tag or label with the full text, the text on a display carton, or a sign or poster, with a copy in the box), and give catalog, mail order and door-to-door sellers copies; or (702.3(b)(2)) post the terms on its website, state the web address and a non-Internet way to request them in the manual or on the product or package, and send a free hard copy on request.

Exemptions (2)

Products bought solely for commercial or industrial use are excluded from this part; warranties that cover only a repairer's workmanship (services) are not covered by the Act (700.1(h)).

“Products which are purchased solely for commercial or industrial use are excluded solely for purposes of this part.”
16 CFR 702.1(b) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

Third-party emblems, seals or insignias promising replacement or refund, with no representation of quality or performance, are exempt from the in-store display duty (702.3(a)(1)) if the third party publishes the 701.3 disclosures and gives them free on written request.

“Paragraph (a)(1) of this section shall not be applicable with respect to statements of general policy on emblems, seals or insignias issued by third parties promising replacement or refund if a consumer product is defective”
16 CFR 702.3(b)(3) (excerpt) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 23 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; versioner date 2026-10-23.

  • It is a consumer product (tangible personal property normally used for personal, family or household purposes) (16 CFR 701.1(b), 702.1(b))
  • You give a written warranty on a consumer product that costs the consumer more than $15, or sell such a product with one (16 CFR 702.3: "The following requirements apply to consumer products actually costing the consumer more than $15.00"; the seller's duties are in 702.3(a), the warrantor's in 702.3(b))

In force since 1 Jan 1977

Applies to products manufactured on or after 1 Jan 1977

Parts 701 and 702 apply only to written warranties on products manufactured after December 31, 1976 (16 CFR 700.12); 702.3 was last revised at 81 FR 63669, Sept. 15, 2016 (online warranty terms option).

“the seller of a consumer product with a written warranty shall make a text of the warranty readily available for examination by the prospective buyer by:”
16 CFR 702.3(a) (excerpt) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)
Registration

Owner, operator or agent in charge of a domestic or foreign facility that manufactures/processes, packs or holds food for US consumption registers the facility with FDA

Registration required

FDA food facility registration (21 CFR 1.225-1.235); renewal every other year Oct 1 to Dec 31 of even-numbered years

Exemptions (2)

Farms; retail food establishments; restaurants; nonprofit food establishments serving consumers; fishing vessels; facilities regulated exclusively by USDA

“This subpart does not apply to the following facilities: (a)”
21 CFR 1.226 · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

Foreign facility whose food undergoes further manufacturing/processing by another facility outside the United States

“(a) A foreign facility, if food from such facility undergoes further manufacturing/processing (including packaging) by another facility outside the United States. A”
21 CFR 1.226(a) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • Operates a food facility or food business
  • Facility exempt from registration (21 CFR 1.226): no

Depends on: operates food facility, facility registration exempt

In force since 10 Oct 2003

Applies to products placed on the market on or after 10 Oct 2003

Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

“You must register your facility under this subpart if you are the owner, operator, or agent in charge of either a domestic or foreign facility,”
1.225(a) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)
Registration

Register before the facility begins to manufacture, process, pack or hold food for US consumption

Registration required

FDA food facility registration before operations begin

The start date is not stated in the text (date unknown).

Later deadlines (2)

4 Jan 2020: Registration and renewal must be submitted electronically

“Beginning on January 4, 2020, you must submit your registration or registration renewal to FDA electronically”
21 CFR 1.231(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

1 Oct 2020: Registration must include facility's FDA-acceptable UFI

“Beginning October 1, 2020, the facility's UFI recognized as acceptable by FDA”
21 CFR 1.232(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • Your role: Manufacturer or Distributor or Fulfilment service provider

Depends on: economic operator role

In force, start date unknown

In force no later than 2026-10-07 (the stored eCFR version date); earlier commencement is not stated in the published text.

“You must register before your facility begins to manufacture, process, pack, or hold food for consumption in the United States. You may authorize an individual to register the facility on your behalf.”
21 CFR 1.230(a) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)
Registration

Renew the food facility registration every other year between Oct 1 and Dec 31 of each even-numbered year

Registration required

FDA food facility registration renewal, biennially in even-numbered years

The start date is not stated in the text (date unknown).

Later deadlines (2)

4 Jan 2020: Registration and renewal must be submitted electronically

“Beginning on January 4, 2020, you must submit your registration or registration renewal to FDA electronically”
21 CFR 1.231(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

1 Oct 2020: Registration must include facility's FDA-acceptable UFI

“Beginning October 1, 2020, the facility's UFI recognized as acceptable by FDA”
21 CFR 1.232(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • Your role: Manufacturer or Distributor or Fulfilment service provider

Depends on: economic operator role

In force, start date unknown

In force no later than 2026-10-07 (the stored eCFR version date); earlier commencement is not stated in the published text.

“You must submit a registration renewal containing the information required under § 1.232 every other year, during the period beginning on October”
21 CFR 1.230(b) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)
Notification

Prior notice of imported food submitted to FDA and confirmed before arrival (2 h road, 4 h rail or air, 8 h water)

Notification to FDA

prior notice of imported food: identity, manufacturer, shipper, grower, country of origin, arrival information

Exemptions (1)

Personal-use food, gifts made by an individual, and food imported then exported without leaving the port are outside the subpart

“Notwithstanding paragraph (a) of this section, this subpart does not apply to: (1) Food for an individual's personal use when it is carried by or otherwise accompanies the individual when arriving in the United States;”
21 CFR 1.277(b) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart I (eCFR, versioner 2026-10-07)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

  • Imported into the market of sale

Depends on: imported

In force since 7 Nov 2008

Applies to products imported on or after 7 Nov 2008

Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

“you must submit the prior notice to FDA and the prior notice submission must be confirmed by FDA for review as follows: (1) If”
1.279(a) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart I (eCFR, versioner 2026-10-07)(opens in a new tab)
  • Notification
    PFAS as defined in United States (federal)

    Notification to US EPA through the Central Data Exchange (CDX), the PFAS 8(a)(7) reporting tool (§705.35)

    Submit the §705.15 information (or, for article importers, the §705.18(a) streamlined form) during the submission period. §705.20(a): the submission period begins January 31, 2027, or 60 days following the date EPA announces in the Federal Register under paragraph (c), whichever is earlier, and lasts six months. §705.20(b): a small manufacturer (40 CFR 704.3) reporting exclusively as an article importer under §705.18(a) has twelve months from the same start. §705.25: keep the records that document what was reported for 5 years beginning on the last day of the submission period.

    Exemptions (2)

    Reporting is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste

    “Reporting under this part is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste.”
    §705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

    Reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage

    “Additionally, reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage.”
    §705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
    Later deadlines (1)

    31 Jan 2027: Submission period starts on this date at the latest (earlier if EPA announces a date: 60 days after it); it lasts six months, or twelve months for a small manufacturer reporting only as an article importer

    “the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier, and last for six months.”
    §705.20(a) (excerpt) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
    Penalty

    Failure or refusal to submit the information, or to keep and give access to the records, is unlawful under TSCA section 15(3); a person who violates TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted (no penalty amount is stated in this part)

    “TSCA section 16 provides that any person who violates a provision of TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted.”
    §705.1(b) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 22 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-22 per the eCFR (title 40 up to date as of 2026-10-22). Section 705.20 carries the amendment 91 FR 18789, Apr. 13, 2026.

    Applies when
    • Your role: Manufacturer or Importer
    • You manufactured (including imported) a PFAS, or an article containing one, for commercial purposes at any time from January 1, 2011 through December 31, 2022

    Depends on: economic operator role

    Effective

    Takes effect 31 Jan 2027

    Applies to products manufactured on or after 31 Jan 2027

    Stated in §705.20(a)-(b): “the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier”. Paragraph (c): “EPA intends to publish a document in the Federal Register announcing the submission period date and revising or removing this paragraph (c).” The period had not begun on the date this row was made (2026-10-26); the date is the latest start the text allows.

    Source
    “All information reported to EPA in response to the requirements of this part must be submitted during the applicable submission period.”
    §705.20(a) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
  • Applies when

    Every product in the category

    Effective

    Dates run from 15 Mar 1977 to 7 Sep 2005

    Each rule has its own date; open a target.

    Source

    Example: Calamus and its derivatives

    “§ 189.110 Calamus and its derivatives. (a) Calamus is the dried rhizome of Acorus calamus L. It has been used as a flavoring compound, especially as the oil or extract.”
    Parts 172-189 substance sections, 21 CFR 189.110, Subpart Substances Generally Prohibited From Direct Addition or Use as Human Food · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
  • Ban
    Flectol H

    Banned

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • It contains Flectol H
    Effective

    In force since 15 Mar 1977

    Applies to products sold on or after 15 Mar 1977

    Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

    Source
    “§ 189.220 Flectol H. (a) Flectol H is the chemical 1,2-dihydro-2,2,4-trimethylquinoline, polymerized, C12H15N. It is a synthetic chemical not found in natural products, and has been used as a component of food packaging adhesives.”
    Parts 172-189 substance sections, 21 CFR 189.220, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
  • Ban
    Mercaptoimidazoline and 2-mercaptoimidazoline

    Banned

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • It contains mercaptoimidazoline or 2-mercaptoimidazoline
    Effective

    In force since 15 Mar 1977

    Applies to products sold on or after 15 Mar 1977

    Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

    Source
    “§ 189.250 Mercaptoimidazoline and 2-mercaptoimidazoline. (a) Mercaptoimidazoline and 2-mercaptoimidazoline both have the molecular formula C3H6N2S. They are synthetic chemicals not found in natural products and have been used in the production of rubber articles that may come into contact with food.”
    Parts 172-189 substance sections, 21 CFR 189.250, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
  • Ban
    4,4′-Methylenebis (2-chloroanaline)

    Banned

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • It contains 4,4′-methylenebis (2-chloroanaline)
    Effective

    In force since 15 Mar 1977

    Applies to products sold on or after 15 Mar 1977

    Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

    Source
    “§ 189.280 4,4′-Methylenebis (2-chloroanaline). (a) 4,4′-Methylenebis (2-chloroanaline) has the molecular formula, C13H12Cl2N2. It is a synthetic chemical not found in natural products and has been used as a polyurethane curing agent and as a component of food packaging adhesives and polyurethane resins.”
    Parts 172-189 substance sections, 21 CFR 189.280, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
  • Ban
    Hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins

    Banned

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • It contains hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins
    Effective

    In force since 17 Feb 1989

    Applies to products sold on or after 17 Feb 1989

    Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

    Source
    “§ 189.300 Hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins. (a) Hydrogenated 4,4′-isopropylidene-diphenolphosphite ester resins are the condensation product of 1 mole of triphenyl phosphite and 1.5 moles of hydrogenated 4,4′-isopropylidene-diphenol such that the finished resins have a molecular weight in the range of 2,400 to 3,000. They are synthetic chemicals not found in natural products and have been used as antioxidants and as stabilizers in vinyl chloride polymer resins when such polymer resins are used in the manufacture of rigid vinyl chloride polymer bottles.”
    Parts 172-189 substance sections, 21 CFR 189.300, Subpart Substances Prohibited From Indirect Addition to Human Food Through Food-Contact Surfaces · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 189 (eCFR, version of 2026-10-07)(opens in a new tab)
  • Ban

    If it is offered for sale under the name of another food.

    Banned

    The start date is not stated in the text (date unknown).

    Official text, current to 31 Dec 2024. United States Code, 2024 Edition, published by GPO; amendments enacted after the edition are not in this text.

    Applies when

    Every product in the category

    Effective

    In force, start date unknown

    In force no later than 2024-01-01 (the stored 2024 edition's date); earlier commencement is not stated in the published text.

    Source
    “If it is offered for sale under the name of another food.”
    343(b) · fetched 2026-10-09US Government Publishing Office (GovInfo, USCODE-2024 edition): 21 U.S.C. 343 (2024 Edition)(opens in a new tab)
  • Notification
    PFAS as defined in United States (federal)

    Notification to US EPA through the Central Data Exchange (CDX), the PFAS 8(a)(7) reporting tool (§705.35)

    Persons who manufactured a PFAS, including as an importer, for commercial purposes at any period from January 1, 2011 through the end of the last calendar year before November 13, 2023 must report to EPA. §705.1(a): “This part specifies reporting and recordkeeping procedures for manufacturers (including importers) of per- and polyfluoroalkyl substances (hereafter referred to as PFAS) under section 8(a)(7) of the Toxic Substances Control Act (TSCA).” §705.5: “The requirements of this part apply to all chemical substances and mixtures containing a chemical substance (including articles) that are a PFAS, consistent with the definition of PFAS at § 705.3.” §705.18(a): an importer of an article that contains a PFAS may use a streamlined article-importer form for each year since January 1, 2011 in which the PFAS was imported in an article. PFAS is defined in §705.3 by three structural sub-structures; this check lists the rule for a product only if it contains a PFAS.

    Exemptions (2)

    Reporting is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste

    “Reporting under this part is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste.”
    §705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

    Reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage

    “Additionally, reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage.”
    §705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

    The start date is not stated in the text (date unknown).

    Penalty

    Failure or refusal to submit the information, or to keep and give access to the records, is unlawful under TSCA section 15(3); a person who violates TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted (no penalty amount is stated in this part)

    “TSCA section 16 provides that any person who violates a provision of TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted.”
    §705.1(b) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 22 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-22 per the eCFR (title 40 up to date as of 2026-10-22). Section 705.20 carries the amendment 91 FR 18789, Apr. 13, 2026.

    Applies when
    • Your role: Manufacturer or Importer
    • You manufactured (including imported) a PFAS, or an article containing one, for commercial purposes at any time from January 1, 2011 through December 31, 2022

    Depends on: economic operator role

    Effective

    In force, start date unknown

    The text names November 13, 2023 only as the end of the look-back window in §705.10 (“the last calendar year prior to November 13, 2023”); it states no operative date of its own, so that date stands in. The one-time report covers each year since January 1, 2011; when it is due is in the §705.20 row.

    Source
    “Persons who have manufactured for commercial purposes a chemical substance identified in § 705.5 at any period from January 1, 2011, through the end of the last calendar year prior to November 13, 2023, except as described in § 705.12, is subject to the requirements of this part.”
    §705.10 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
  • Conformity

    A claim that the product or its package is free of BPA or does not contain or use BPA.

    Must meet the conditions of A claim that the product is free of BPA must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if BPA has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: BPA-free
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
    §260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
  • Conformity

    A compostable claim made for the product or its package.

    Must meet the conditions of Do not misrepresent, directly or by implication, that the product or package is compostable.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: compostable
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product or package is compostable.”
    §260.7(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.7(opens in a new tab)
  • Conformity

    A degradable or biodegradable claim (including oxo-degradable, oxo-biodegradable and photodegradable claims) made for the product or its package.

    Must meet the conditions of Do not misrepresent, directly or by implication, that the product or package is degradable, biodegradable, oxo-degradable, oxo-biodegradable or photodegradable.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: biodegradable
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product or package is degradable, biodegradable, oxo-degradable, oxo-biodegradable, or photodegradable.”
    §260.8(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.8(opens in a new tab)
  • Conformity

    A claim that the product or its package is free of formaldehyde or does not contain or use formaldehyde.

    Must meet the conditions of A claim that the product is free of formaldehyde must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if formaldehyde has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: formaldehyde-free
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
    §260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
  • Conformity

    A general environmental benefit claim (for example "eco-friendly" or "green") made for the product or its package.

    Must meet the conditions of Do not misrepresent, directly or by implication, that the product, package or service offers a general environmental benefit.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: eco-friendly
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product, package, or service offers a general environmental benefit.”
    §260.4(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.4(opens in a new tab)
  • Conformity

    A claim that the product or its package is free of lead or does not contain or use lead.

    Must meet the conditions of A claim that the product is free of lead must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if lead has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: lead-free
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
    §260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
  • Conformity

    A non-toxic claim made for the product or its package.

    Must meet the conditions of Do not misrepresent, directly or by implication, that the product, package or service is non-toxic. Qualify a non-toxic claim clearly and prominently to the extent necessary to avoid deception.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: non-toxic
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product, package, or service is non-toxic. Non-toxic claims should be clearly and prominently qualified to the extent necessary to avoid deception.”
    §260.10(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.10(opens in a new tab)
  • Conformity

    A claim that the product or its package is free of PFAS or does not contain or use PFAS.

    Must meet the conditions of A claim that the product is free of PFAS must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if PFAS has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: PFAS-free
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
    §260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
  • Conformity

    A claim that the product or its package is free of PTFE or does not contain or use PTFE.

    Must meet the conditions of A claim that the product is free of PTFE must be truthful and be clearly and prominently qualified to the extent necessary to avoid deception. Even a truthful claim may be deceptive if the product contains or uses substances that pose the same or similar environmental risks, or if PTFE has not been associated with the product category. A free-of claim can be appropriate for a trace amount only if the level is no more than an acknowledged trace contaminant or background level, its presence does not cause material harm that consumers typically associate with the substance, and it was not added intentionally. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: PTFE-free
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “It is deceptive to misrepresent, directly or by implication, that a product, package, or service is free of, or does not contain or use, a substance.”
    §260.9(a) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.9(opens in a new tab)
  • Conformity

    A recyclable claim made for the product or its package.

    Must meet the conditions of Market the item as recyclable only if it can be collected, separated or otherwise recovered from the waste stream through an established recycling program for reuse or for use in making another item. Make an unqualified claim only when recycling facilities are available to a substantial majority (at least 60 percent) of consumers or communities where the item is sold; otherwise qualify the claim. Qualify which portions are recyclable when only some components are, and do not call the item recyclable if any component, or its shape or size, significantly limits recycling. These Guides are the FTC's guidance on how Section 5 of the FTC Act applies to environmental claims; they do not ban the claim, but the FTC can act against a claim that is inconsistent with them.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: recyclable
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the current Guides (October 11, 2012); it states no separate effective date.

    Source
    “A product or package should not be marketed as recyclable unless it can be collected, separated, or otherwise recovered from the waste stream through an established recycling program”
    §260.12(a) (excerpt) · fetched 2026-10-22US FTC via eCFR: 16 CFR 260.12(opens in a new tab)
  • Conformity

    A label that represents the product as Made in the United States without qualification.

    Must meet the conditions of Label a product as Made in the United States only if its final assembly or processing occurs in the United States, all significant processing that goes into it occurs in the United States, and all or virtually all of its ingredients or components are made and sourced in the United States. The same applies to a seal, mark, tag or stamp in a mail order catalog or mail order promotional material. A violation is treated as a violation of a trade regulation rule under section 18 of the FTC Act.

    The start date is not stated in the text (date unknown).

    Consolidated text (not the authentic legal edition), current to 20 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-20 per the eCFR.

    Applies when
    • Claim: Made in USA
    Effective

    In force, start date unknown

    The text states only the Federal Register publication date of the rule (July 14, 2021); it states no separate effective date.

    Source
    “all significant processing that goes into the product occurs in the United States, and all or virtually all ingredients or components of the product are made and sourced in the United States.”
    §323.2 (excerpt) · fetched 2026-10-22US FTC via eCFR: 16 CFR 323.2(opens in a new tab)
  • Disclosure

    If you give a written warranty, put all its terms in one clear document: who and what is covered, what you will do, how long, how to claim, and the required State-rights statements

    Disclosure to buyer

    Written warranty terms (16 CFR 701.3(a)): a warrantor who gives a written warranty on a consumer product costing the consumer more than $15.00 must clearly and conspicuously disclose, in a single document in simple and readily understood language: (1) who the warranty is extended to, if limited to the original purchaser or otherwise; (2) the products, parts or components covered and, where needed, excluded; (3) what the warrantor will do on a defect or failure, and what it will pay for or provide; (4) when the term starts if not on the purchase date, and how long it lasts; (5) step by step how to claim, with the warrantor's name and mailing address or responsible department, or a free telephone number; (6) any informal dispute settlement mechanism (part 703); (7) any limit on the duration of implied warranties, with "Some States do not allow limitations on how long an implied warranty lasts, so the above limitation may not apply to you."; (8) any exclusion or limit on incidental or consequential damages, with its State-law statement; (9) "This warranty gives you specific legal rights, and you may also have other rights which vary from State to State." If return of a registration card is a condition of coverage, the warranty must say so (701.4).

    Exemptions (2)

    Products bought solely for commercial or industrial use are excluded from this part; warranties that cover only a repairer's workmanship (services) are not covered by the Act (700.1(h)).

    “Products which are purchased solely for commercial or industrial use are excluded solely for purposes of this part.”
    16 CFR 701.1(b) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

    Third-party emblems, seals or insignias promising replacement or refund, with no representation of quality or performance, are exempt from (a)(1)-(9) if the third party publishes the disclosures in each issue of a general-circulation publication and gives them free on written request.

    “Paragraphs (a) (1) through (9) of this section shall not be applicable with respect to statements of general policy on emblems, seals or insignias issued by third parties promising replacement or refund if a consumer product is defective”
    16 CFR 701.3(b) (excerpt) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 23 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; versioner date 2026-10-23.

    Applies when
    • It is a consumer product (tangible personal property normally used for personal, family or household purposes) (16 CFR 701.1(b), 702.1(b))
    • You give a written warranty on a consumer product that costs the consumer more than $15 (16 CFR 701.2: the rules apply to "written warranties on consumer products actually costing the consumer more than $15.00"; 701.1(h): a warrantor is "any supplier, manufacturer, or other person who gives or offers to give a written warranty")
    Effective

    In force since 1 Jan 1977

    Applies to products manufactured on or after 1 Jan 1977

    Parts 701 and 702 apply only to written warranties on products manufactured after December 31, 1976 (16 CFR 700.12); 702.3 was last revised at 81 FR 63669, Sept. 15, 2016 (online warranty terms option).

    Source
    “Any warrantor warranting to a consumer by means of a written warranty a consumer product actually costing the consumer more than $15.00 shall clearly and conspicuously disclose in a single document in simple and readily understood language, the following items of information:”
    16 CFR 701.3(a) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)
  • Disclosure

    Make the written warranty's text available to the buyer before the sale (in store, catalog or online listing, door to door); the warrantor supplies the text or posts it online

    Disclosure to buyer

    Pre-sale availability of written warranty terms (16 CFR 702.3), for consumer products costing the consumer more than $15.00. Seller (702.3(a)): make the warranty text readily available before sale by displaying it close to the product, or by furnishing it on request with signs telling buyers it is available. Catalog and mail order sellers, including any offer whose ordering does not need a visit to the seller (702.3(c)): give the full text, or the warrantor's web address plus where to request a free copy, beside the product description or in a referenced section. Door-to-door sellers: say before the sale that the warranties may be inspected (702.3(d)). Warrantor (702.3(b)(1)): give sellers the warranty materials (a copy with every product, a tag or label with the full text, the text on a display carton, or a sign or poster, with a copy in the box), and give catalog, mail order and door-to-door sellers copies; or (702.3(b)(2)) post the terms on its website, state the web address and a non-Internet way to request them in the manual or on the product or package, and send a free hard copy on request.

    Exemptions (2)

    Products bought solely for commercial or industrial use are excluded from this part; warranties that cover only a repairer's workmanship (services) are not covered by the Act (700.1(h)).

    “Products which are purchased solely for commercial or industrial use are excluded solely for purposes of this part.”
    16 CFR 702.1(b) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

    Third-party emblems, seals or insignias promising replacement or refund, with no representation of quality or performance, are exempt from the in-store display duty (702.3(a)(1)) if the third party publishes the 701.3 disclosures and gives them free on written request.

    “Paragraph (a)(1) of this section shall not be applicable with respect to statements of general policy on emblems, seals or insignias issued by third parties promising replacement or refund if a consumer product is defective”
    16 CFR 702.3(b)(3) (excerpt) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 23 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; versioner date 2026-10-23.

    Applies when
    • It is a consumer product (tangible personal property normally used for personal, family or household purposes) (16 CFR 701.1(b), 702.1(b))
    • You give a written warranty on a consumer product that costs the consumer more than $15, or sell such a product with one (16 CFR 702.3: "The following requirements apply to consumer products actually costing the consumer more than $15.00"; the seller's duties are in 702.3(a), the warrantor's in 702.3(b))
    Effective

    In force since 1 Jan 1977

    Applies to products manufactured on or after 1 Jan 1977

    Parts 701 and 702 apply only to written warranties on products manufactured after December 31, 1976 (16 CFR 700.12); 702.3 was last revised at 81 FR 63669, Sept. 15, 2016 (online warranty terms option).

    Source
    “the seller of a consumer product with a written warranty shall make a text of the warranty readily available for examination by the prospective buyer by:”
    16 CFR 702.3(a) (excerpt) · fetched 2026-10-27US FTC via eCFR: 15 U.S.C. 2301 ff.; 16 CFR 700.1, 701.2, 701.3, 702.3(opens in a new tab)
  • Registration

    Owner, operator or agent in charge of a domestic or foreign facility that manufactures/processes, packs or holds food for US consumption registers the facility with FDA

    Registration required

    FDA food facility registration (21 CFR 1.225-1.235); renewal every other year Oct 1 to Dec 31 of even-numbered years

    Exemptions (2)

    Farms; retail food establishments; restaurants; nonprofit food establishments serving consumers; fishing vessels; facilities regulated exclusively by USDA

    “This subpart does not apply to the following facilities: (a)”
    21 CFR 1.226 · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

    Foreign facility whose food undergoes further manufacturing/processing by another facility outside the United States

    “(a) A foreign facility, if food from such facility undergoes further manufacturing/processing (including packaging) by another facility outside the United States. A”
    21 CFR 1.226(a) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • Operates a food facility or food business
    • Facility exempt from registration (21 CFR 1.226): no

    Depends on: operates food facility, facility registration exempt

    Effective

    In force since 10 Oct 2003

    Applies to products placed on the market on or after 10 Oct 2003

    Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

    Source
    “You must register your facility under this subpart if you are the owner, operator, or agent in charge of either a domestic or foreign facility,”
    1.225(a) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)
  • Registration

    Register before the facility begins to manufacture, process, pack or hold food for US consumption

    Registration required

    FDA food facility registration before operations begin

    The start date is not stated in the text (date unknown).

    Later deadlines (2)

    4 Jan 2020: Registration and renewal must be submitted electronically

    “Beginning on January 4, 2020, you must submit your registration or registration renewal to FDA electronically”
    21 CFR 1.231(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

    1 Oct 2020: Registration must include facility's FDA-acceptable UFI

    “Beginning October 1, 2020, the facility's UFI recognized as acceptable by FDA”
    21 CFR 1.232(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • Your role: Manufacturer or Distributor or Fulfilment service provider

    Depends on: economic operator role

    Effective

    In force, start date unknown

    In force no later than 2026-10-07 (the stored eCFR version date); earlier commencement is not stated in the published text.

    Source
    “You must register before your facility begins to manufacture, process, pack, or hold food for consumption in the United States. You may authorize an individual to register the facility on your behalf.”
    21 CFR 1.230(a) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)
  • Registration

    Renew the food facility registration every other year between Oct 1 and Dec 31 of each even-numbered year

    Registration required

    FDA food facility registration renewal, biennially in even-numbered years

    The start date is not stated in the text (date unknown).

    Later deadlines (2)

    4 Jan 2020: Registration and renewal must be submitted electronically

    “Beginning on January 4, 2020, you must submit your registration or registration renewal to FDA electronically”
    21 CFR 1.231(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

    1 Oct 2020: Registration must include facility's FDA-acceptable UFI

    “Beginning October 1, 2020, the facility's UFI recognized as acceptable by FDA”
    21 CFR 1.232(a)(2) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • Your role: Manufacturer or Distributor or Fulfilment service provider

    Depends on: economic operator role

    Effective

    In force, start date unknown

    In force no later than 2026-10-07 (the stored eCFR version date); earlier commencement is not stated in the published text.

    Source
    “You must submit a registration renewal containing the information required under § 1.232 every other year, during the period beginning on October”
    21 CFR 1.230(b) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart H (eCFR, versioner 2026-10-07)(opens in a new tab)
  • Notification

    Prior notice of imported food submitted to FDA and confirmed before arrival (2 h road, 4 h rail or air, 8 h water)

    Notification to FDA

    prior notice of imported food: identity, manufacturer, shipper, grower, country of origin, arrival information

    Exemptions (1)

    Personal-use food, gifts made by an individual, and food imported then exported without leaving the port are outside the subpart

    “Notwithstanding paragraph (a) of this section, this subpart does not apply to: (1) Food for an individual's personal use when it is carried by or otherwise accompanies the individual when arriving in the United States;”
    21 CFR 1.277(b) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart I (eCFR, versioner 2026-10-07)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 7 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-07 per the eCFR.

    Applies when
    • Imported into the market of sale

    Depends on: imported

    Effective

    In force since 7 Nov 2008

    Applies to products imported on or after 7 Nov 2008

    Date stated in the published text: the first Federal Register date of the section history note (or of the part Source line where the section has none), used as the provision date.

    Source
    “you must submit the prior notice to FDA and the prior notice submission must be confirmed by FDA for review as follows: (1) If”
    1.279(a) (excerpt) · fetched 2026-10-09US National Archives / Office of the Federal Register (eCFR): 21 CFR Part 1 subpart I (eCFR, versioner 2026-10-07)(opens in a new tab)

Gaps

Markets without rules for this category

We have no rules for this category in these markets. That doesn't mean none apply, so a check here says Not covered, never clear.

ClaraDB gives a verdict only for PFAS state laws for cookware and bakeware, California Proposition 65 consumer-product warning check for BPA, BPS, formaldehyde, styrene, antimony trioxide, vinyl acetate, lead and cadmium, California Proposition 65 warning check for candles and ceramicware (lead, cadmium, formaldehyde, acetaldehyde, benzene, naphthalene, carbon monoxide, benzo[a]pyrene), US packaging EPR producer size thresholds (California, Colorado, Maryland, Minnesota, Oregon, Washington) for a brand-owning manufacturer, US lead in children's products and furniture (lead paint and total lead content), US lead in toys and child care articles (lead paint and total lead content), US lead in children's products (other) and bags (lead paint and total lead content), US phthalates in children's toys and child care articles (DEHP, DBP, BBP, DINP, DIBP, DPENP, DHEXP, DCHP) and US children's product certificate and tracking label for children's tableware (AI-checked, quotes verified word for word). Every other answer shows the laws and quotes found without saying whether they apply. Not checked: Consumer electronics (FCC equipment authorization, 47 CFR Parts 2 and 15, energy rules). What ClaraDB has checked

Show 2 markets
Market
Coverage
Main sources; no modeled rule is scoped to this category. Not covered: other rules that may apply.
Main sources; no modeled rule is scoped to this category. Not covered: other rules that may apply.
  • Coverage
    Main sources; no modeled rule is scoped to this category. Not covered: other rules that may apply.
  • Coverage
    Main sources; no modeled rule is scoped to this category. Not covered: other rules that may apply.

Facts

What we need to know about your product

Some rules depend on details of your product. Until you tell us, a check says Needs answers and asks for what's missing.

Show 74 facts
Depends on
Markets
Rules
Whether the listed substance or group is present
EU, GB, US, US-CA, US-VT
7,504
Eu food category code
EU, GB
5,149
Number of employees at the seller
US-CA
972
Contaminant food category
EU, GB
804
Sold prepacked
EU, GB, JP, KR, US
161
Economic operator role
EU, GB, JP, KR, US
50
Imported
EU, GB, JP, KR, US
41
Allergens present
EU, GB, JP, KR, US
36
Special storage required
EU, GB, JP, KR
35
Glass bottle reusable unlabelled
EU, GB
32
Contains gmo
JP, KR
31
Component content declared
KR
28
Precaution statement required
KR
28
Operates food facility
EU, GB, JP, US
25
Jp processed food
JP
18
Jp general use food
JP
18
List of ingredients present
EU, GB
11
Materials
US
11
Irradiated
EU, GB, KR, US
10
Beverage
EU, GB
8
Annex ix sold by number or loss
EU, GB
8
Prepacked for direct sale
GB
6
Facility registration exempt
US
6
Frozen
KR
5
Qualified facility
US
5
Facility registration required
US
5
Annual gross revenue usd
US-CO, US-MD, US-MN, US-OR, US-WA
5
Contains glycyrrhizinic acid
EU, GB
4
Liquorice in name or ingredients
EU, GB
4
Sweeteners present
EU, GB
4
Small package area cm2
EU, GB
4
Whether it is sold online
EU, GB
4
Name of food refers to allergen
EU, GB
4
Use difficult without instructions
EU, GB
4
Alcohol abv
EU, GB
4
Annex v exempt product
EU, GB
4
Offered by distance communication
GB
4
Aspartame present
EU, GB, KR
3
Food additive present
EU, GB, JP
3
Oem consignment manufactured
KR
3
Added polyols over 10 percent
EU, GB
2
Caffeine mg per l
EU, GB
2
Engineered nanomaterial ingredient
EU, GB
2
Refrigerated
EU, GB
2
Post opening storage appropriate
EU, GB
2
Label implies different origin
EU, GB
2
Country of origin stated
EU, GB
2
Operator knows noncompliant
EU, GB
2
Chemical detoxification applied
EU, GB
2
Jp annex 20 food
JP
2
Jp permit business type
JP
2
Canned or bottled
KR
2
Distributed in exporting country
KR
2
Restaurant or retail service
US
2
Coating type
US
2
Sorting destined lot
EU
1
Contains meat
GB
1
Schedule 3 food
GB
1
Oral disclosure intended
GB
1
Gmo annex 17 ingredient
JP
1
Additive undesignated
JP
1
Sulfiting agent added
US
1
Nutrition claim
US
1
Chemical preservative added
US
1
Imitation food claim
US
1
Gluten free claim
US
1
Direct additive used
US
1
Ca gross sales usd
US-CA
1
Packaging tons co
US-CO
1
Packaging tons md
US-MD
1
Packaging tons mn
US-MN
1
Packaging tonnes or
US-OR
1
Fluorine treated container
US-VT
1
Packaging tons wa
US-WA
1
  • Whether the listed substance or group is present
    Markets
    EU, GB, US, US-CA, US-VT
    Rules
    7,504
  • Eu food category code
    Markets
    EU, GB
    Rules
    5,149
  • Number of employees at the seller
    Markets
    US-CA
    Rules
    972
  • Contaminant food category
    Markets
    EU, GB
    Rules
    804
  • Sold prepacked
    Markets
    EU, GB, JP, KR, US
    Rules
    161
  • Economic operator role
    Markets
    EU, GB, JP, KR, US
    Rules
    50
  • Imported
    Markets
    EU, GB, JP, KR, US
    Rules
    41
  • Allergens present
    Markets
    EU, GB, JP, KR, US
    Rules
    36
  • Special storage required
    Markets
    EU, GB, JP, KR
    Rules
    35
  • Glass bottle reusable unlabelled
    Markets
    EU, GB
    Rules
    32
  • Contains gmo
    Markets
    JP, KR
    Rules
    31
  • Component content declared
    Markets
    KR
    Rules
    28
  • Precaution statement required
    Markets
    KR
    Rules
    28
  • Operates food facility
    Markets
    EU, GB, JP, US
    Rules
    25
  • Jp processed food
    Markets
    JP
    Rules
    18
  • Jp general use food
    Markets
    JP
    Rules
    18
  • List of ingredients present
    Markets
    EU, GB
    Rules
    11
  • Materials
    Markets
    US
    Rules
    11
  • Irradiated
    Markets
    EU, GB, KR, US
    Rules
    10
  • Beverage
    Markets
    EU, GB
    Rules
    8
  • Annex ix sold by number or loss
    Markets
    EU, GB
    Rules
    8
  • Prepacked for direct sale
    Markets
    GB
    Rules
    6
  • Facility registration exempt
    Markets
    US
    Rules
    6
  • Frozen
    Markets
    KR
    Rules
    5
  • Qualified facility
    Markets
    US
    Rules
    5
  • Facility registration required
    Markets
    US
    Rules
    5
  • Annual gross revenue usd
    Markets
    US-CO, US-MD, US-MN, US-OR, US-WA
    Rules
    5
  • Contains glycyrrhizinic acid
    Markets
    EU, GB
    Rules
    4
  • Liquorice in name or ingredients
    Markets
    EU, GB
    Rules
    4
  • Sweeteners present
    Markets
    EU, GB
    Rules
    4
  • Small package area cm2
    Markets
    EU, GB
    Rules
    4
  • Whether it is sold online
    Markets
    EU, GB
    Rules
    4
  • Name of food refers to allergen
    Markets
    EU, GB
    Rules
    4
  • Use difficult without instructions
    Markets
    EU, GB
    Rules
    4
  • Alcohol abv
    Markets
    EU, GB
    Rules
    4
  • Annex v exempt product
    Markets
    EU, GB
    Rules
    4
  • Offered by distance communication
    Markets
    GB
    Rules
    4
  • Aspartame present
    Markets
    EU, GB, KR
    Rules
    3
  • Food additive present
    Markets
    EU, GB, JP
    Rules
    3
  • Oem consignment manufactured
    Markets
    KR
    Rules
    3
  • Added polyols over 10 percent
    Markets
    EU, GB
    Rules
    2
  • Caffeine mg per l
    Markets
    EU, GB
    Rules
    2
  • Engineered nanomaterial ingredient
    Markets
    EU, GB
    Rules
    2
  • Refrigerated
    Markets
    EU, GB
    Rules
    2
  • Post opening storage appropriate
    Markets
    EU, GB
    Rules
    2
  • Label implies different origin
    Markets
    EU, GB
    Rules
    2
  • Country of origin stated
    Markets
    EU, GB
    Rules
    2
  • Operator knows noncompliant
    Markets
    EU, GB
    Rules
    2
  • Chemical detoxification applied
    Markets
    EU, GB
    Rules
    2
  • Jp annex 20 food
    Markets
    JP
    Rules
    2
  • Jp permit business type
    Markets
    JP
    Rules
    2
  • Canned or bottled
    Markets
    KR
    Rules
    2
  • Distributed in exporting country
    Markets
    KR
    Rules
    2
  • Restaurant or retail service
    Markets
    US
    Rules
    2
  • Coating type
    Markets
    US
    Rules
    2
  • Sorting destined lot
    Markets
    EU
    Rules
    1
  • Contains meat
    Markets
    GB
    Rules
    1
  • Schedule 3 food
    Markets
    GB
    Rules
    1
  • Oral disclosure intended
    Markets
    GB
    Rules
    1
  • Gmo annex 17 ingredient
    Markets
    JP
    Rules
    1
  • Additive undesignated
    Markets
    JP
    Rules
    1
  • Sulfiting agent added
    Markets
    US
    Rules
    1
  • Nutrition claim
    Markets
    US
    Rules
    1
  • Chemical preservative added
    Markets
    US
    Rules
    1
  • Imitation food claim
    Markets
    US
    Rules
    1
  • Gluten free claim
    Markets
    US
    Rules
    1
  • Direct additive used
    Markets
    US
    Rules
    1
  • Ca gross sales usd
    Markets
    US-CA
    Rules
    1
  • Packaging tons co
    Markets
    US-CO
    Rules
    1
  • Packaging tons md
    Markets
    US-MD
    Rules
    1
  • Packaging tons mn
    Markets
    US-MN
    Rules
    1
  • Packaging tonnes or
    Markets
    US-OR
    Rules
    1
  • Fluorine treated container
    Markets
    US-VT
    Rules
    1
  • Packaging tons wa
    Markets
    US-WA
    Rules
    1

Changes

Upcoming changes

Rules for this category that start in the next 24 months, or are proposed or on hold.

Show 33 upcoming changes
Requirement
Applies when
Effective
Source
WarningUS-CA
N-Methyl-N-Formylhydrazine (CAS 758-17-8)

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to N-Methyl-N-Formylhydrazine, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 8 Dec 2026

Applies to products sold on or after 8 Dec 2026

Listed 2025-12-08 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
N-Methyl-N-Formylhydrazine
Type of toxicity
cancer
Listed by
the State's Qualified Experts (SQE)
CAS No.
758-17-8
Date listed
8 Dec 2025

Prop 65 list row: N-Methyl-N-Formylhydrazine · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Bisphenol S (BPS) (CAS 80-09-1)

Warning required when exposure exceeds the threshold (no MADL listed for this row)

This product can expose you to Bisphenol S (BPS), which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required for a reproductive toxicant where the exposure will produce no observable effect at 1,000 times the level in question (at or below the MADL).

“a warning is not required if the business causing the exposure can demonstrate that the exposure will produce no observable effect, even at 1,000 times the level in question.”
Appendix A (summary), Exposures that will produce no observable reproductive effect (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 8 Dec 2026

Applies to products sold on or after 8 Dec 2026

Listed 2025-12-08 (developmental). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Bisphenol S (BPS)
Type of toxicity
developmental toxicity
Listed by
the State's Qualified Experts (SQE)
CAS No.
80-09-1
Date listed
8 Dec 2025

Prop 65 list row: Bisphenol S (BPS) · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Tacrolimus (CAS 104987-11-3)

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Tacrolimus, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Tacrolimus
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
104987-11-3
Date listed
17 Jul 2026

Prop 65 list row: Tacrolimus · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Hydrochlorothiazide

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Hydrochlorothiazide, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Hydrochlorothiazide
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
58-93-5; 125727-50-6; 8049-49-8
Date listed
17 Jul 2026

Prop 65 list row: Hydrochlorothiazide · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Voriconazole

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Voriconazole, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Voriconazole
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
137234-62-9; 188416-29-7; 173967-54-9
Date listed
17 Jul 2026

Prop 65 list row: Voriconazole · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
WarningUS-CA
Welding Fumes

Warning required when exposure exceeds the threshold (no NSRL listed for this row)

This product can expose you to Welding Fumes, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

Exemptions (1)

No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

  • Seller has 10 or more employees
  • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

Depends on: number of employees at the seller

Takes effect 17 Jul 2027

Applies to products sold on or after 17 Jul 2027

Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

Chemical
Welding Fumes
Type of toxicity
cancer
Listed by
the Labor Code (LC)
CAS No.
none given
Date listed
17 Jul 2026

Prop 65 list row: Welding Fumes · fetched 2026-10-08

California OEHHA: 27 CCR 27001(opens in a new tab)
NotificationUS
PFAS as defined in United States (federal)

Notification to US EPA through the Central Data Exchange (CDX), the PFAS 8(a)(7) reporting tool (§705.35)

Submit the §705.15 information (or, for article importers, the §705.18(a) streamlined form) during the submission period. §705.20(a): the submission period begins January 31, 2027, or 60 days following the date EPA announces in the Federal Register under paragraph (c), whichever is earlier, and lasts six months. §705.20(b): a small manufacturer (40 CFR 704.3) reporting exclusively as an article importer under §705.18(a) has twelve months from the same start. §705.25: keep the records that document what was reported for 5 years beginning on the last day of the submission period.

Exemptions (2)

Reporting is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste

“Reporting under this part is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste.”
§705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

Reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage

“Additionally, reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage.”
§705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
Later deadlines (1)

31 Jan 2027: Submission period starts on this date at the latest (earlier if EPA announces a date: 60 days after it); it lasts six months, or twelve months for a small manufacturer reporting only as an article importer

“the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier, and last for six months.”
§705.20(a) (excerpt) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
Penalty

Failure or refusal to submit the information, or to keep and give access to the records, is unlawful under TSCA section 15(3); a person who violates TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted (no penalty amount is stated in this part)

“TSCA section 16 provides that any person who violates a provision of TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted.”
§705.1(b) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 22 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-22 per the eCFR (title 40 up to date as of 2026-10-22). Section 705.20 carries the amendment 91 FR 18789, Apr. 13, 2026.

  • Your role: Manufacturer or Importer
  • You manufactured (including imported) a PFAS, or an article containing one, for commercial purposes at any time from January 1, 2011 through December 31, 2022

Depends on: economic operator role

Takes effect 31 Jan 2027

Applies to products manufactured on or after 31 Jan 2027

Stated in §705.20(a)-(b): “the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier”. Paragraph (c): “EPA intends to publish a document in the Federal Register announcing the submission period date and revising or removing this paragraph (c).” The period had not begun on the date this row was made (2026-10-26); the date is the latest start the text allows.

“All information reported to EPA in response to the requirements of this part must be submitted during the applicable submission period.”
§705.20(a) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
ConformityKR

Food additives: the 식품첨가물의 기준 및 규격 decide whether an additive is acceptable

Must meet the conditions of I. 총칙 3. 1): acceptability of a food additive is judged by the 총칙, 제조기준, 일반사용기준, 품목별 기준 및 규격 and 일반시험법 of the notice

Official text, current to 13 Jul 2026. MFDS notice 2026-50 full text (발령 2026-07-13) from law.go.kr; it takes effect 2028-01-01 (시행), so it may not be the text in force.

Every product in the category

Takes effect 1 Jan 2028

Applies to products sold on or after 1 Jan 2028

Notice 2026-50 (발령 2026-07-13) carries [시행일 : ‘28.1.1.] per its published text; the version in force before 2028-01-01 is not stored, so no earlier dates are covered.

“이 고시에 실린 식품첨가물의 적․부는 총칙, 제조기준, 일반사용기준, 품목별 기준 및 규격, 일반시험법의 규정에 따라 판정한다”
I. 총칙 3. 1) · fetched 2026-10-09Ministry of Food and Drug Safety (attachment via law.go.kr flDownload): 식품의약품안전처고시 제2026-50호 식품첨가물의 기준 및 규격 (발령 2026-07-13, 시행 2028-01-01)(opens in a new tab)
Label x 84KR

84 rules from 식품등의 표시기준 (MFDS notice 2026-37)

Label required

Show targets (40 of 84)
  • 사) 영양성분(한식메주, 한식된장은 제외)
  • 바) 원재료명
  • 바) 영양성분
  • 아) 용기ㆍ포장 재질
  • 아) 용기ㆍ포장 재질
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시
  • 아) 용기ㆍ포장 재질
  • (가) 부정ㆍ불량식품신고표시
  • 자) 품목보고번호
  • (1) 부정ㆍ불량식품신고표시
  • 아) 용기ㆍ포장 재질
  • 자) 품목보고번호
  • 사) 영양성분
  • 아) 용기ㆍ포장 재질
  • 자) 품목보고번호
  • 아) 용기ㆍ포장 재질
  • 아) 용기ㆍ포장 재질
  • 자) 품목보고번호
  • 바) 원재료명
  • 바) 원재료명
  • 자) 품목보고번호
  • 사) 영양성분
  • 자) 품목보고번호
  • 자) 품목보고번호
  • 바) 원재료명
  • 바) 원재료명
  • (6) 원재료명
  • 아) 용기ㆍ포장 재질
  • 바) 원재료명
  • 바) 원재료명
  • (1) 부정ㆍ불량식품신고표시
  • (1) 부정ㆍ불량식품신고표시

The remaining targets are listed on the substances page.

Every product in the category

1 Jan 2028

Each rule has its own date; open a target.

Example: 사) 영양성분(한식메주, 한식된장은 제외)

“사) 영양성분(한식메주, 한식된장은 제외)”
Ⅲ. 1. 타. 2) 사) · fetched 2026-10-09Ministry of Food and Drug Safety / National Law Information Center (law.go.kr): 식품의약품안전처고시 제2026-37호 (발령 2026-05-12, 시행 2028-01-01)(opens in a new tab)
Label x 15KR

15 rules from 식품등의 표시기준 (MFDS notice 2026-37)

Label required

Show targets (15 of 15)
  • 카) 보관방법(해당 경우에 한함)
  • (11) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 마) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • 카) 보관방법(해당 경우에 한함)
  • Special storage conditions are required

Depends on: special storage required

1 Jan 2028

Each rule has its own date; open a target.

Example: 카) 보관방법(해당 경우에 한함)

“카) 보관방법(해당 경우에 한함)”
Ⅲ. 1. 다. 2) 카) · fetched 2026-10-09Ministry of Food and Drug Safety / National Law Information Center (law.go.kr): 식품의약품안전처고시 제2026-37호 (발령 2026-05-12, 시행 2028-01-01)(opens in a new tab)
  • WarningUS-CA
    N-Methyl-N-Formylhydrazine (CAS 758-17-8)

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to N-Methyl-N-Formylhydrazine, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 8 Dec 2026

    Applies to products sold on or after 8 Dec 2026

    Listed 2025-12-08 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    N-Methyl-N-Formylhydrazine
    Type of toxicity
    cancer
    Listed by
    the State's Qualified Experts (SQE)
    CAS No.
    758-17-8
    Date listed
    8 Dec 2025

    Prop 65 list row: N-Methyl-N-Formylhydrazine · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Bisphenol S (BPS) (CAS 80-09-1)

    Warning required when exposure exceeds the threshold (no MADL listed for this row)

    This product can expose you to Bisphenol S (BPS), which is known to the State of California to cause birth defects or other reproductive harm. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required for a reproductive toxicant where the exposure will produce no observable effect at 1,000 times the level in question (at or below the MADL).

    “a warning is not required if the business causing the exposure can demonstrate that the exposure will produce no observable effect, even at 1,000 times the level in question.”
    Appendix A (summary), Exposures that will produce no observable reproductive effect (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 8 Dec 2026

    Applies to products sold on or after 8 Dec 2026

    Listed 2025-12-08 (developmental). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Bisphenol S (BPS)
    Type of toxicity
    developmental toxicity
    Listed by
    the State's Qualified Experts (SQE)
    CAS No.
    80-09-1
    Date listed
    8 Dec 2025

    Prop 65 list row: Bisphenol S (BPS) · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Tacrolimus (CAS 104987-11-3)

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Tacrolimus, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Tacrolimus
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    104987-11-3
    Date listed
    17 Jul 2026

    Prop 65 list row: Tacrolimus · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Hydrochlorothiazide

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Hydrochlorothiazide, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Hydrochlorothiazide
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    58-93-5; 125727-50-6; 8049-49-8
    Date listed
    17 Jul 2026

    Prop 65 list row: Hydrochlorothiazide · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Voriconazole

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Voriconazole, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Voriconazole
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    137234-62-9; 188416-29-7; 173967-54-9
    Date listed
    17 Jul 2026

    Prop 65 list row: Voriconazole · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • WarningUS-CA
    Welding Fumes

    Warning required when exposure exceeds the threshold (no NSRL listed for this row)

    This product can expose you to Welding Fumes, which is known to the State of California to cause cancer. For more information go to www.P65Warnings.ca.gov.

    Exemptions (1)

    No warning is required where the exposure poses no significant risk of cancer (at or below the NSRL).

    a warning is not required if the business causing the exposure can demonstrate that the exposure occurs at a level that poses “no significant risk
    Appendix A (summary), Exposures that pose no significant risk of cancer (excerpt) · fetched 2026-10-08California OAG / OEHHA: 27 CCR 27001(opens in a new tab)

    Official text, current to 31 Jul 2026. OEHHA's own Prop 65 list (XLSX), list dated July 31, 2026.

    Applies when
    • Seller has 10 or more employees
    • Your business has 10 or more employees and the product knowingly and intentionally exposes someone in California to this chemical

    Depends on: number of employees at the seller

    Effective

    Takes effect 17 Jul 2027

    Applies to products sold on or after 17 Jul 2027

    Listed 2026-07-17 (cancer). Grace period: "Proposition 65 warning requirements do not apply until 12 months after the chemical has been listed" (Appendix A); listing date plus 12 months.

    Source
    Chemical
    Welding Fumes
    Type of toxicity
    cancer
    Listed by
    the Labor Code (LC)
    CAS No.
    none given
    Date listed
    17 Jul 2026

    Prop 65 list row: Welding Fumes · fetched 2026-10-08

    California OEHHA: 27 CCR 27001(opens in a new tab)
  • NotificationUS
    PFAS as defined in United States (federal)

    Notification to US EPA through the Central Data Exchange (CDX), the PFAS 8(a)(7) reporting tool (§705.35)

    Submit the §705.15 information (or, for article importers, the §705.18(a) streamlined form) during the submission period. §705.20(a): the submission period begins January 31, 2027, or 60 days following the date EPA announces in the Federal Register under paragraph (c), whichever is earlier, and lasts six months. §705.20(b): a small manufacturer (40 CFR 704.3) reporting exclusively as an article importer under §705.18(a) has twelve months from the same start. §705.25: keep the records that document what was reported for 5 years beginning on the last day of the submission period.

    Exemptions (2)

    Reporting is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste

    “Reporting under this part is not required for the import of municipal solid waste streams for the purpose of disposal or destruction of the waste.”
    §705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

    Reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage

    “Additionally, reporting is not required for a Federal agency which imports PFAS when it is not for any immediate or eventual commercial advantage.”
    §705.12 · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
    Later deadlines (1)

    31 Jan 2027: Submission period starts on this date at the latest (earlier if EPA announces a date: 60 days after it); it lasts six months, or twelve months for a small manufacturer reporting only as an article importer

    “the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier, and last for six months.”
    §705.20(a) (excerpt) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
    Penalty

    Failure or refusal to submit the information, or to keep and give access to the records, is unlawful under TSCA section 15(3); a person who violates TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted (no penalty amount is stated in this part)

    “TSCA section 16 provides that any person who violates a provision of TSCA section 15 is liable to the United States for a civil penalty and may be criminally prosecuted.”
    §705.1(b) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 22 Oct 2026. eCFR is an editorial compilation of the CFR, not the official legal edition; current to 2026-10-22 per the eCFR (title 40 up to date as of 2026-10-22). Section 705.20 carries the amendment 91 FR 18789, Apr. 13, 2026.

    Applies when
    • Your role: Manufacturer or Importer
    • You manufactured (including imported) a PFAS, or an article containing one, for commercial purposes at any time from January 1, 2011 through December 31, 2022

    Depends on: economic operator role

    Effective

    Takes effect 31 Jan 2027

    Applies to products manufactured on or after 31 Jan 2027

    Stated in §705.20(a)-(b): “the submission period shall begin January 31, 2027, or 60 days following the date provided in paragraph (c) of this section, whichever is earlier”. Paragraph (c): “EPA intends to publish a document in the Federal Register announcing the submission period date and revising or removing this paragraph (c).” The period had not begun on the date this row was made (2026-10-26); the date is the latest start the text allows.

    Source
    “All information reported to EPA in response to the requirements of this part must be submitted during the applicable submission period.”
    §705.20(a) · fetched 2026-10-26US EPA via eCFR: 40 CFR 705(opens in a new tab)
  • ConformityKR

    Food additives: the 식품첨가물의 기준 및 규격 decide whether an additive is acceptable

    Must meet the conditions of I. 총칙 3. 1): acceptability of a food additive is judged by the 총칙, 제조기준, 일반사용기준, 품목별 기준 및 규격 and 일반시험법 of the notice

    Official text, current to 13 Jul 2026. MFDS notice 2026-50 full text (발령 2026-07-13) from law.go.kr; it takes effect 2028-01-01 (시행), so it may not be the text in force.

    Applies when

    Every product in the category

    Effective

    Takes effect 1 Jan 2028

    Applies to products sold on or after 1 Jan 2028

    Notice 2026-50 (발령 2026-07-13) carries [시행일 : ‘28.1.1.] per its published text; the version in force before 2028-01-01 is not stored, so no earlier dates are covered.

    Source
    “이 고시에 실린 식품첨가물의 적․부는 총칙, 제조기준, 일반사용기준, 품목별 기준 및 규격, 일반시험법의 규정에 따라 판정한다”
    I. 총칙 3. 1) · fetched 2026-10-09Ministry of Food and Drug Safety (attachment via law.go.kr flDownload): 식품의약품안전처고시 제2026-50호 식품첨가물의 기준 및 규격 (발령 2026-07-13, 시행 2028-01-01)(opens in a new tab)
  • Label x 84KR

    84 rules from 식품등의 표시기준 (MFDS notice 2026-37)

    Label required

    Show targets (40 of 84)
    • 사) 영양성분(한식메주, 한식된장은 제외)
    • 바) 원재료명
    • 바) 영양성분
    • 아) 용기ㆍ포장 재질
    • 아) 용기ㆍ포장 재질
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시
    • 아) 용기ㆍ포장 재질
    • (가) 부정ㆍ불량식품신고표시
    • 자) 품목보고번호
    • (1) 부정ㆍ불량식품신고표시
    • 아) 용기ㆍ포장 재질
    • 자) 품목보고번호
    • 사) 영양성분
    • 아) 용기ㆍ포장 재질
    • 자) 품목보고번호
    • 아) 용기ㆍ포장 재질
    • 아) 용기ㆍ포장 재질
    • 자) 품목보고번호
    • 바) 원재료명
    • 바) 원재료명
    • 자) 품목보고번호
    • 사) 영양성분
    • 자) 품목보고번호
    • 자) 품목보고번호
    • 바) 원재료명
    • 바) 원재료명
    • (6) 원재료명
    • 아) 용기ㆍ포장 재질
    • 바) 원재료명
    • 바) 원재료명
    • (1) 부정ㆍ불량식품신고표시
    • (1) 부정ㆍ불량식품신고표시

    The remaining targets are listed on the substances page.

    Applies when

    Every product in the category

    Effective

    1 Jan 2028

    Each rule has its own date; open a target.

    Source

    Example: 사) 영양성분(한식메주, 한식된장은 제외)

    “사) 영양성분(한식메주, 한식된장은 제외)”
    Ⅲ. 1. 타. 2) 사) · fetched 2026-10-09Ministry of Food and Drug Safety / National Law Information Center (law.go.kr): 식품의약품안전처고시 제2026-37호 (발령 2026-05-12, 시행 2028-01-01)(opens in a new tab)
  • Label x 15KR

    15 rules from 식품등의 표시기준 (MFDS notice 2026-37)

    Label required

    Show targets (15 of 15)
    • 카) 보관방법(해당 경우에 한함)
    • (11) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 마) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    • 카) 보관방법(해당 경우에 한함)
    Applies when
    • Special storage conditions are required

    Depends on: special storage required

    Effective

    1 Jan 2028

    Each rule has its own date; open a target.

    Source

    Example: 카) 보관방법(해당 경우에 한함)

    “카) 보관방법(해당 경우에 한함)”
    Ⅲ. 1. 다. 2) 카) · fetched 2026-10-09Ministry of Food and Drug Safety / National Law Information Center (law.go.kr): 식품의약품안전처고시 제2026-37호 (발령 2026-05-12, 시행 2028-01-01)(opens in a new tab)
All dated changes

Records

Recalls and alerts

Recalls, safety alerts and Prop 65 notices that name Cheese, with a link to the original. A Prop 65 notice is a claim by the sender, not a ruling.

13 records dated 6 Jun 2023 to 2 Oct 2026. Most recent shown.

Show the 8 most recent records

See also

Related categories

Alerts

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