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Cosmetics and personal care

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We track 6,916 rules for these in 20 of 21 markets, including California's Prop 65 list of 883 chemicals. Check your product free, no account needed.

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Cosmetics and personal care / Hair care and colour / Hair styling

Leave-on gels, sprays, mousses, waxes and treatments (often aerosol).

Rules

Rules by market

Open a market to read its rules for this category.

European Union2,271 rulesCoverage: Main sources, from 18 May 2026
Main sources, from 18 May 2026 · What is covered

European Union: main sources stored. Modelled: Reg. 1223/2009 Annexes II (prohibited); III (restricted); IV (colourants); V (preservatives); VI (UV filters) and Art. 19 labelling; Arts. 4 to 13: Responsible Person, safety assessment and safety report (CPSR), product information file (PIF), CPNP notification. Not stored: CLP classification and labelling of cosmetic mixtures; REACH Annex XVII entries beyond cosmetics (e.g. microplastics Reg. 2023/2055); national rules (e.g. French recycling labels, German language rules); claims criteria (Reg. 655/2013); packaging law (PPWR); Annex III-VI entries adopted after the stored consolidation.

Requirement
Applies when
Effective
Source
Conformity

Art. 6(3)

Must meet the conditions of Art. 6(3): do not make a non-conforming product available until it is brought into conformity; ensure corrective measures, withdrawal or recall for products already made available

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“they shall not make the product available on the market until it has been brought into conformity with the applicable requirements”
Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

Art. 6(4)

Must meet the conditions of Art. 6(4): storage or transport conditions under the distributor's responsibility do not jeopardise compliance

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“storage or transport conditions do not jeopardise its compliance with the requirements set out in this Regulation”
Art. 6(4) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Distributor informs RP and authorities of risk

Notification to Responsible person and competent authorities

Details of non-compliance and corrective measures taken

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Furthermore, where the cosmetic product presents a risk to human health, distributors shall immediately inform the responsible person and the competent national authorities of the Member States”
Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Distributor that translates labelling notifies the Commission

Notification to European Commission (CPNP)

Category, names in both Member States, Member State of availability, distributor name and address, responsible person

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 13(3): 'As from 11 July 2013' (stated in the provision); Art. 40(2) is consistent.

“a distributor who makes available in a Member State a cosmetic product already placed on the market in another Member State and translates, on his own initiative, any element of the labelling of that product in order to comply with national law, shall submit, by electronic means, the following information to the Commission”
Art. 13(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Test

Distributors verify labelling, language and durability before making available

Test required

Distributor verification before making a product available: labelling information (Art. 19(1)(a), (e), (g), 19(3)-(4)), language requirements and date of minimum durability

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products distributed on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Before making a cosmetic product available on the market distributors shall verify that:”
Art. 6(2) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Label

Mandatory label element: nominal content

Label required

Nominal content at the time of packaging by weight or volume

Exemptions (1)

Free samples and single-application packs; pre-packages normally sold as a number of items where the number appears on the packaging or is easy to see from outside

“free samples and single-application packs”
Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Net content at least 5 mL

Depends on: net content ml

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“the nominal content at the time of packaging, given by weight or by volume, except in the case of packaging containing less than five grams or five millilitres, free samples and single-application packs”
Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Notification of cosmetic products containing nanomaterials six months before placing on the market

Notification to European Commission

Nanomaterial identification (IUPAC name and descriptors), specification (particle size, physical and chemical properties), estimated annual quantity, toxicological profile, safety data for the product category, reasonably foreseeable exposure conditions; six months before placing on the market

Exemptions (2)

Not applicable to cosmetic products containing nanomaterials in conformity with Annex III

“shall not apply to cosmetic products containing nanomaterials that are in conformity with the requirements set out in Annex III”
Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

Art. 16 does not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14, unless expressly specified

“do not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14”
Art. 16(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Contains a nanomaterial
  • Your role: Manufacturer or Importer

Depends on: contains nanomaterial, economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the first subparagraph of Art. 16(3) applies from 11 July 2013 with the Regulation; only the second subparagraph (products already on the market, notification between 11 January 2013 and 11 July 2013) applies from 11 January 2013 and is a transitional duty not listed as a separate rule.

“cosmetic products containing nanomaterials shall be notified to the Commission by the responsible person by electronic means six months prior to being placed on the market”
Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity

A no-animal-test claim is allowed only where no animal tests were carried out or commissioned

Must meet the conditions of Art. 20(3): a no-animal-testing claim only if neither the manufacturer nor its suppliers carried out or commissioned animal tests on the finished product, prototype or ingredients, or used ingredients tested on animals by others for developing new cosmetic products

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Claim: not tested on animals

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“to the fact that no animal tests have been carried out only if the manufacturer and his suppliers have not carried out or commissioned any animal tests”
Art. 20(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Update of notified information when it changes

Notification to European Commission (CPNP)

Update, without delay, of any changed information notified under Art. 13(1), (3) or (4)

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer or Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Where any of the information set out in paragraphs 1, 3 and 4 changes, the responsible person or the distributor shall provide an update without delay.”
Art. 13(7) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Notification

Notify serious undesirable effects

Notification to Competent authority of the Member State where the serious undesirable effect occurred

All serious undesirable effects known or reasonably expected to be known, the name of the product enabling identification, and any corrective measures taken

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer or Distributor

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“In the event of serious undesirable effects, the responsible person and distributors shall without delay notify the following to the competent authority of the Member State where the serious undesirable effect occurred:”
Art. 23(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Disclosure

PIF accessible to authority at address on label, in understandable language

Disclosure to authority

Make the product information file readily accessible at the address on the label, in a language easily understood by the authority

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“The responsible person shall make the product information file readily accessible in electronic or other format at his address indicated on the label to the competent authority of the Member State in which the file is kept.”
Art. 11(3) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Disclosure

Public access to composition and undesirable effect data

Disclosure to consumer

Qualitative and quantitative composition (quantitative information limited to hazardous substances under CLP Art. 3), for perfume compositions the name, code number and supplier, and existing data on undesirable and serious undesirable effects, made easily accessible to the public

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“the responsible person shall ensure that the qualitative and quantitative composition of the cosmetic product and, in the case of perfume and aromatic compositions, the name and code number of the composition and the identity of the supplier, as well as existing data on undesirable effects and serious undesirable effects”
Art. 21 (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Declaration

Responsible person keeps a product information file

Declaration required

Product information file, kept for ten years after the last batch was placed on the market, containing the product description, the safety report (Art. 10(1)), the manufacturing method and GMP statement, proof of the claimed effect where justified, and animal-testing data (Art. 11(2))

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“When a cosmetic product is placed on the market, the responsible person shall keep a product information file for it.”
Art. 11(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Registration

A responsible person within the Community

Registration required

Designation of a responsible person established in the Union for each cosmetic product (Art. 4)

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

Every product in the category

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“Only cosmetic products for which a legal or natural person is designated within the Community as ‘responsible person’ shall be placed on the market.”
Art. 4(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Test

Safety assessment and cosmetic product safety report before placing on the market

Test required

Safety assessment of the cosmetic product before placing it on the market and a cosmetic product safety report in accordance with Annex I

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Your role: Manufacturer or Importer

Depends on: economic operator role

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“the responsible person shall, prior to placing a cosmetic product on the market, ensure that the cosmetic product has undergone a safety assessment on the basis of the relevant information and that a cosmetic product safety report is set up in accordance with Annex I.”
Art. 10(1) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
Conformity
Polyacrylamides

Must meet the conditions of Annex III entry 66: (a) Body- leave-on products | (a) Maximum residual acrylamide content 0,1 mg/kg

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Leave-on product

Depends on: rinse off

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

From the consolidated text: Polyacrylamides · (a) Body- leave-on products

Conformity
Methylphenylenediamines, their N- substituted derivatives and their salts, with the exception of the substance listed under reference numbers 9 a and 9 b of this Annex and the substances listed under reference numbers 364, 413, 1144, 1310, 1313 and 1507 of Annex II

Must meet the conditions of Annex III entry 9: (b) Professional use

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

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • For professional use only

Depends on: professional use

In force, start date unknown

No date for this row is stated in the published text (consolidation marker M36; the amending act's application date is not printed). In force no later than 2026-05-18 (the date of the version ClaraDB holds); earlier commencement is not stated in the published text.

“(b) Professional use”
Annex III entry 9 (l1-cond) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Label
Methylphenylenediamines, their N- substituted derivatives and their salts, with the exception of the substance listed under reference numbers 9 a and 9 b of this Annex and the substances listed under reference numbers 364, 413, 1144, 1310, 1313 and 1507 of Annex II

Label required

(b) To be printed on the label:

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

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • For professional use only

Depends on: professional use

In force, start date unknown

No date for this row is stated in the published text (consolidation marker M36; the amending act's application date is not printed). In force no later than 2026-05-18 (the date of the version ClaraDB holds); earlier commencement is not stated in the published text.

“(b) To be printed on the label:”
Annex III entry 9 (l1-wording) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Disclosure

Identify supply chain on authority request, three years

Disclosure to authority

Identify distributors supplied (responsible person) or supplier and customers (distributor) for three years after batch made available

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

Every product in the category

In force since 11 Jul 2013

Applies to products placed on the market on or after 11 Jul 2013

Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

“responsible persons shall identify the distributors to whom they supply the cosmetic product,”
Art. 7 (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    Art. 6(3)

    Must meet the conditions of Art. 6(3): do not make a non-conforming product available until it is brought into conformity; ensure corrective measures, withdrawal or recall for products already made available

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “they shall not make the product available on the market until it has been brought into conformity with the applicable requirements”
    Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    Art. 6(4)

    Must meet the conditions of Art. 6(4): storage or transport conditions under the distributor's responsibility do not jeopardise compliance

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “storage or transport conditions do not jeopardise its compliance with the requirements set out in this Regulation”
    Art. 6(4) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Distributor informs RP and authorities of risk

    Notification to Responsible person and competent authorities

    Details of non-compliance and corrective measures taken

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Furthermore, where the cosmetic product presents a risk to human health, distributors shall immediately inform the responsible person and the competent national authorities of the Member States”
    Art. 6(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Distributor that translates labelling notifies the Commission

    Notification to European Commission (CPNP)

    Category, names in both Member States, Member State of availability, distributor name and address, responsible person

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 13(3): 'As from 11 July 2013' (stated in the provision); Art. 40(2) is consistent.

    Source
    “a distributor who makes available in a Member State a cosmetic product already placed on the market in another Member State and translates, on his own initiative, any element of the labelling of that product in order to comply with national law, shall submit, by electronic means, the following information to the Commission”
    Art. 13(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Test

    Distributors verify labelling, language and durability before making available

    Test required

    Distributor verification before making a product available: labelling information (Art. 19(1)(a), (e), (g), 19(3)-(4)), language requirements and date of minimum durability

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products distributed on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Before making a cosmetic product available on the market distributors shall verify that:”
    Art. 6(2) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Label

    Mandatory label element: nominal content

    Label required

    Nominal content at the time of packaging by weight or volume

    Exemptions (1)

    Free samples and single-application packs; pre-packages normally sold as a number of items where the number appears on the packaging or is easy to see from outside

    “free samples and single-application packs”
    Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Net content at least 5 mL

    Depends on: net content ml

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “the nominal content at the time of packaging, given by weight or by volume, except in the case of packaging containing less than five grams or five millilitres, free samples and single-application packs”
    Art. 19(1)(b) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Notification of cosmetic products containing nanomaterials six months before placing on the market

    Notification to European Commission

    Nanomaterial identification (IUPAC name and descriptors), specification (particle size, physical and chemical properties), estimated annual quantity, toxicological profile, safety data for the product category, reasonably foreseeable exposure conditions; six months before placing on the market

    Exemptions (2)

    Not applicable to cosmetic products containing nanomaterials in conformity with Annex III

    “shall not apply to cosmetic products containing nanomaterials that are in conformity with the requirements set out in Annex III”
    Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

    Art. 16 does not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14, unless expressly specified

    “do not apply to nanomaterials used as colorants, UV-filters or preservatives regulated under Article 14”
    Art. 16(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Contains a nanomaterial
    • Your role: Manufacturer or Importer

    Depends on: contains nanomaterial, economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the first subparagraph of Art. 16(3) applies from 11 July 2013 with the Regulation; only the second subparagraph (products already on the market, notification between 11 January 2013 and 11 July 2013) applies from 11 January 2013 and is a transitional duty not listed as a separate rule.

    Source
    “cosmetic products containing nanomaterials shall be notified to the Commission by the responsible person by electronic means six months prior to being placed on the market”
    Art. 16(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity

    A no-animal-test claim is allowed only where no animal tests were carried out or commissioned

    Must meet the conditions of Art. 20(3): a no-animal-testing claim only if neither the manufacturer nor its suppliers carried out or commissioned animal tests on the finished product, prototype or ingredients, or used ingredients tested on animals by others for developing new cosmetic products

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Claim: not tested on animals
    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “to the fact that no animal tests have been carried out only if the manufacturer and his suppliers have not carried out or commissioned any animal tests”
    Art. 20(3) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Update of notified information when it changes

    Notification to European Commission (CPNP)

    Update, without delay, of any changed information notified under Art. 13(1), (3) or (4)

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer or Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Where any of the information set out in paragraphs 1, 3 and 4 changes, the responsible person or the distributor shall provide an update without delay.”
    Art. 13(7) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Notification

    Notify serious undesirable effects

    Notification to Competent authority of the Member State where the serious undesirable effect occurred

    All serious undesirable effects known or reasonably expected to be known, the name of the product enabling identification, and any corrective measures taken

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer or Distributor

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “In the event of serious undesirable effects, the responsible person and distributors shall without delay notify the following to the competent authority of the Member State where the serious undesirable effect occurred:”
    Art. 23(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Disclosure

    PIF accessible to authority at address on label, in understandable language

    Disclosure to authority

    Make the product information file readily accessible at the address on the label, in a language easily understood by the authority

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “The responsible person shall make the product information file readily accessible in electronic or other format at his address indicated on the label to the competent authority of the Member State in which the file is kept.”
    Art. 11(3) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Disclosure

    Public access to composition and undesirable effect data

    Disclosure to consumer

    Qualitative and quantitative composition (quantitative information limited to hazardous substances under CLP Art. 3), for perfume compositions the name, code number and supplier, and existing data on undesirable and serious undesirable effects, made easily accessible to the public

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “the responsible person shall ensure that the qualitative and quantitative composition of the cosmetic product and, in the case of perfume and aromatic compositions, the name and code number of the composition and the identity of the supplier, as well as existing data on undesirable effects and serious undesirable effects”
    Art. 21 (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Declaration

    Responsible person keeps a product information file

    Declaration required

    Product information file, kept for ten years after the last batch was placed on the market, containing the product description, the safety report (Art. 10(1)), the manufacturing method and GMP statement, proof of the claimed effect where justified, and animal-testing data (Art. 11(2))

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “When a cosmetic product is placed on the market, the responsible person shall keep a product information file for it.”
    Art. 11(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Registration

    A responsible person within the Community

    Registration required

    Designation of a responsible person established in the Union for each cosmetic product (Art. 4)

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when

    Every product in the category

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “Only cosmetic products for which a legal or natural person is designated within the Community as ‘responsible person’ shall be placed on the market.”
    Art. 4(1) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Test

    Safety assessment and cosmetic product safety report before placing on the market

    Test required

    Safety assessment of the cosmetic product before placing it on the market and a cosmetic product safety report in accordance with Annex I

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Your role: Manufacturer or Importer

    Depends on: economic operator role

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “the responsible person shall, prior to placing a cosmetic product on the market, ensure that the cosmetic product has undergone a safety assessment on the basis of the relevant information and that a cosmetic product safety report is set up in accordance with Annex I.”
    Art. 10(1) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
  • Conformity
    Polyacrylamides

    Must meet the conditions of Annex III entry 66: (a) Body- leave-on products | (a) Maximum residual acrylamide content 0,1 mg/kg

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Leave-on product

    Depends on: rinse off

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    No row-level date in the consolidated text for this entry; it applies from the Regulation's application date (Art. 40: 11 July 2013). Later amendments (the ▼M markers) are not dated row by row in the text.

    Source

    From the consolidated text: Polyacrylamides · (a) Body- leave-on products

  • Conformity
    Methylphenylenediamines, their N- substituted derivatives and their salts, with the exception of the substance listed under reference numbers 9 a and 9 b of this Annex and the substances listed under reference numbers 364, 413, 1144, 1310, 1313 and 1507 of Annex II

    Must meet the conditions of Annex III entry 9: (b) Professional use

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

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • For professional use only

    Depends on: professional use

    Effective

    In force, start date unknown

    No date for this row is stated in the published text (consolidation marker M36; the amending act's application date is not printed). In force no later than 2026-05-18 (the date of the version ClaraDB holds); earlier commencement is not stated in the published text.

    Source
    “(b) Professional use”
    Annex III entry 9 (l1-cond) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
  • Label
    Methylphenylenediamines, their N- substituted derivatives and their salts, with the exception of the substance listed under reference numbers 9 a and 9 b of this Annex and the substances listed under reference numbers 364, 413, 1144, 1310, 1313 and 1507 of Annex II

    Label required

    (b) To be printed on the label:

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

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • For professional use only

    Depends on: professional use

    Effective

    In force, start date unknown

    No date for this row is stated in the published text (consolidation marker M36; the amending act's application date is not printed). In force no later than 2026-05-18 (the date of the version ClaraDB holds); earlier commencement is not stated in the published text.

    Source
    “(b) To be printed on the label:”
    Annex III entry 9 (l1-wording) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
  • Disclosure

    Identify supply chain on authority request, three years

    Disclosure to authority

    Identify distributors supplied (responsible person) or supplier and customers (distributor) for three years after batch made available

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when

    Every product in the category

    Effective

    In force since 11 Jul 2013

    Applies to products placed on the market on or after 11 Jul 2013

    Art. 40(2): the Regulation applies from 11 July 2013; this article is not among the exceptions listed there (Art. 15(1)-(2), 14/31/32 as needed for Art. 15, and the second subparagraph of Art. 16(3)).

    Source
    “responsible persons shall identify the distributors to whom they supply the cosmetic product,”
    Art. 7 (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 (consolidated 2026-05-18)(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 1 market
Market
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 36 facts
Depends on
Markets
Rules
Whether the listed substance or group is present
EU, GB, JP, KR, US, US-CA, US-CO, US-CT, US-IL, US-MD, US-ME, US-MN, US-NJ, US-RI, US-VT, US-WA
7,615
Number of employees at the seller
US-CA
972
Rinse off
EU, GB, JP, KR, US-CA
282
Body area
EU, GB, JP, KR
249
Economic operator role
EU, GB, KR, US
90
Sprayable
EU, GB, KR
45
Contains battery
EU, GB, US
39
Intended for children under 3
EU, GB, KR
24
Battery category
EU, GB
22
Otc drug claim
US, US-MN
19
Quasi drug or functional claim
JP, KR
13
Net content ml
EU, GB, KR
10
Professional use
EU, GB, US
9
Battery chemistry
US
9
Aerosol dispenser
JP, KR, US
8
Customised cosmetic
KR
7
Rechargeable
US
6
Animal testing conducted
EU, GB, KR
5
Annual gross revenue usd
US-CO, US-MD, US-MN, US-OR, US-WA
5
Contains nanomaterial
EU, GB
2
Intended for children under 12
KR
2
Single use
KR
2
Button or coin cell
US
2
Distance sale to other member state
EU
1
Imported
KR
1
Cattle derived material
US
1
Uses sunscreen term
US
1
Safety substantiated
US
1
Battery removable
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, JP, KR, US, US-CA, US-CO, US-CT, US-IL, US-MD, US-ME, US-MN, US-NJ, US-RI, US-VT, US-WA
    Rules
    7,615
  • Number of employees at the seller
    Markets
    US-CA
    Rules
    972
  • Rinse off
    Markets
    EU, GB, JP, KR, US-CA
    Rules
    282
  • Body area
    Markets
    EU, GB, JP, KR
    Rules
    249
  • Economic operator role
    Markets
    EU, GB, KR, US
    Rules
    90
  • Sprayable
    Markets
    EU, GB, KR
    Rules
    45
  • Contains battery
    Markets
    EU, GB, US
    Rules
    39
  • Intended for children under 3
    Markets
    EU, GB, KR
    Rules
    24
  • Battery category
    Markets
    EU, GB
    Rules
    22
  • Otc drug claim
    Markets
    US, US-MN
    Rules
    19
  • Quasi drug or functional claim
    Markets
    JP, KR
    Rules
    13
  • Net content ml
    Markets
    EU, GB, KR
    Rules
    10
  • Professional use
    Markets
    EU, GB, US
    Rules
    9
  • Battery chemistry
    Markets
    US
    Rules
    9
  • Aerosol dispenser
    Markets
    JP, KR, US
    Rules
    8
  • Customised cosmetic
    Markets
    KR
    Rules
    7
  • Rechargeable
    Markets
    US
    Rules
    6
  • Animal testing conducted
    Markets
    EU, GB, KR
    Rules
    5
  • Annual gross revenue usd
    Markets
    US-CO, US-MD, US-MN, US-OR, US-WA
    Rules
    5
  • Contains nanomaterial
    Markets
    EU, GB
    Rules
    2
  • Intended for children under 12
    Markets
    KR
    Rules
    2
  • Single use
    Markets
    KR
    Rules
    2
  • Button or coin cell
    Markets
    US
    Rules
    2
  • Distance sale to other member state
    Markets
    EU
    Rules
    1
  • Imported
    Markets
    KR
    Rules
    1
  • Cattle derived material
    Markets
    US
    Rules
    1
  • Uses sunscreen term
    Markets
    US
    Rules
    1
  • Safety substantiated
    Markets
    US
    Rules
    1
  • Battery removable
    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 49 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)
BanEU
Triphenyl Phosphate (CAS 115-86-6)

Banned

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

Every product in the category

Takes effect 1 Jan 2027

Applies to products placed on the market on or after 1 Jan 2027

Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

From the consolidated text: Triphenyl Phosphate (13) · 115-86-6 · 204-112-2

LimitEU
Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

Limit 0.5 % (content basis)

In the finished (ready for use) cosmetic product. Maximum concentration cell: (b) 0,5 %. Field of application: (b) Rinse-off skin and hair products (except shower gel/bath products).

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Rinse-off product

Depends on: rinse off

Takes effect 1 Jan 2027

Applies to products placed on the market on or after 1 Jan 2027

Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

From the consolidated text: (b) Rinse-off skin and hair products (except shower gel/bath products) · (b) 0,5 %

LimitEU
Citral Geranial (CAS 5392-40-5)

Limit 1.2 % (content basis)

In the finished (ready for use) cosmetic product. Maximum concentration cell: (h) 1,2 %. Field of application: (h) Skin and hair rinse-off products.

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Rinse-off product

Depends on: rinse off

Takes effect 1 Jan 2027

Applies to products placed on the market on or after 1 Jan 2027

Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-08-01. The row-level date is read from the annex footnote (EU).

From the consolidated text: (h) Skin and hair rinse-off products · (h) 1,2 %

LimitEU
Acetylated Vetiveria Zizanioides Root Extract (Vetiveria zizanioides, ext., acetylated Oils, vetiver, acetylated; CAS 84082-84-8)

Limit 0.2 % (content basis)

In the finished (ready for use) cosmetic product. Maximum concentration cell: (a) 0,9 % (b) 0,05 % (c) 0,05 % (d) 0,1 % (e) 0,2 %. Field of application: (a) Fragrance products (hydroalcoholic and non-hydroalcoholic, spray and non-spray) (b) Deodorant (c) Make-up products (d) Leave-on products (except (a), (b) and (c)) (e) Rinse-off products. Other: For (a) – (e): stabilised with 1 % alpha-tocopherol (applies to raw materials)..

Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

  • Rinse-off product

Depends on: rinse off

Takes effect 1 Jan 2027

Applies to products placed on the market on or after 1 Jan 2027

Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

“(a) 0,9 % (b) 0,05 % (c) 0,05 % (d) 0,1 % (e) 0,2 %”
Annex III entry 382 (v4e) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(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)
  • BanEU
    Triphenyl Phosphate (CAS 115-86-6)

    Banned

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when

    Every product in the category

    Effective

    Takes effect 1 Jan 2027

    Applies to products placed on the market on or after 1 Jan 2027

    Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

    Source

    From the consolidated text: Triphenyl Phosphate (13) · 115-86-6 · 204-112-2

  • LimitEU
    Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)

    Limit 0.5 % (content basis)

    In the finished (ready for use) cosmetic product. Maximum concentration cell: (b) 0,5 %. Field of application: (b) Rinse-off skin and hair products (except shower gel/bath products).

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Rinse-off product

    Depends on: rinse off

    Effective

    Takes effect 1 Jan 2027

    Applies to products placed on the market on or after 1 Jan 2027

    Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

    Source

    From the consolidated text: (b) Rinse-off skin and hair products (except shower gel/bath products) · (b) 0,5 %

  • LimitEU
    Citral Geranial (CAS 5392-40-5)

    Limit 1.2 % (content basis)

    In the finished (ready for use) cosmetic product. Maximum concentration cell: (h) 1,2 %. Field of application: (h) Skin and hair rinse-off products.

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Rinse-off product

    Depends on: rinse off

    Effective

    Takes effect 1 Jan 2027

    Applies to products placed on the market on or after 1 Jan 2027

    Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-08-01. The row-level date is read from the annex footnote (EU).

    Source

    From the consolidated text: (h) Skin and hair rinse-off products · (h) 1,2 %

  • LimitEU
    Acetylated Vetiveria Zizanioides Root Extract (Vetiveria zizanioides, ext., acetylated Oils, vetiver, acetylated; CAS 84082-84-8)

    Limit 0.2 % (content basis)

    In the finished (ready for use) cosmetic product. Maximum concentration cell: (a) 0,9 % (b) 0,05 % (c) 0,05 % (d) 0,1 % (e) 0,2 %. Field of application: (a) Fragrance products (hydroalcoholic and non-hydroalcoholic, spray and non-spray) (b) Deodorant (c) Make-up products (d) Leave-on products (except (a), (b) and (c)) (e) Rinse-off products. Other: For (a) – (e): stabilised with 1 % alpha-tocopherol (applies to raw materials)..

    Consolidated text (not the authentic legal edition), current to 18 May 2026. EUR-Lex consolidated text: a documentation tool without legal effect; the acts published in the Official Journal are authentic. Consolidated version CELEX 02009R1223-20260518 from the Publications Office, the latest when read.

    Applies when
    • Rinse-off product

    Depends on: rinse off

    Effective

    Takes effect 1 Jan 2027

    Applies to products placed on the market on or after 1 Jan 2027

    Row footnote: products containing the substance shall not be placed on the Union market from 2027-01-01 and not be made available from 2028-07-01. The row-level date is read from the annex footnote (EU).

    Source
    “(a) 0,9 % (b) 0,05 % (c) 0,05 % (d) 0,1 % (e) 0,2 %”
    Annex III entry 382 (v4e) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
All dated changes

Records

Recalls and alerts

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

253 records dated 6 Jan 2023 to 16 Oct 2026. Most recent shown.

Show the 8 most recent records

See also

Related categories

Alerts

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