Cosmetics and personal care
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Cosmetics and personal care / Deodorants and antiperspirants
Underarm products.
Rules
Rules by market
Open a market to read its rules for this category.
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.
Notification of authorities where the product presents a risk to human health
Notification to Competent national authorities of the Member States in which the product was made available and of the Member State where the product information file is readily accessible
Details of the non-compliance and of the 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
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)).
“Furthermore, where the cosmetic product presents a risk to human health, responsible persons shall immediately inform the competent national authorities of the Member States”
Art. 6(1)
Must meet the conditions of Art. 6(1): act with due care in relation to applicable requirements when making a cosmetic product 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)).
“distributors shall act with due care in relation to applicable requirements”
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(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”
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”
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”
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:”
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”
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”
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 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”
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”
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”
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.”
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:”
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.”
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”
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.”
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.”
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.”
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
Annex III entry 66 (cond) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)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”
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:”
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,”
- Notification
Notification of authorities where the product presents a risk to human health
Notification to Competent national authorities of the Member States in which the product was made available and of the Member State where the product information file is readily accessible
Details of the non-compliance and of the 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
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
“Furthermore, where the cosmetic product presents a risk to human health, responsible persons shall immediately inform the competent national authorities of the Member States”
Art. 5(2) (excerpt) · fetched 2026-10-09European Commission / Publications Office (CELLAR): Regulation (EC) No 1223/2009 (consolidated 2026-05-18)(opens in a new tab)
- Conformity
Art. 6(1)
Must meet the conditions of Art. 6(1): act with due care in relation to applicable requirements when making a cosmetic product 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
“distributors shall act with due care in relation to applicable requirements”
Art. 6(1) (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)
- ConformityPolyacrylamides
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
Annex III entry 66 (cond) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
- ConformityMethylphenylenediamines, 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)
- LabelMethylphenylenediamines, 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
- 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
- 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
- 7,526
- Number of employees at the seller
- Markets
- US-CA
- Rules
- 972
- Body area
- Markets
- EU, GB, JP, KR
- Rules
- 249
- Rinse off
- Markets
- EU, GB, JP, KR, US-CA
- Rules
- 235
- Economic operator role
- Markets
- EU, GB, KR, US
- Rules
- 90
- Sprayable
- Markets
- EU, GB, KR
- Rules
- 48
- 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
- Battery chemistry
- Markets
- US
- Rules
- 9
- Aerosol dispenser
- Markets
- JP, KR, US
- Rules
- 8
- Professional use
- Markets
- EU, GB, US
- Rules
- 7
- 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 47 upcoming changes
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
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)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.”
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)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
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)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
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)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
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)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
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)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
Annex II entry 1767 · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)Limit 0.7 % (content basis)
In the finished (ready for use) cosmetic product. Maximum concentration cell: (f) 0,7 %. Field of application: (f) Body lotion.
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.
- Applied to: Body
Depends on: body area
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: (f) Body lotion · (f) 0,7 %
Annex III entry 75 (l5) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)13 rules from Regulation (EC) No 1223/2009 on cosmetic products, Annexes II-VI (consolidated)
Limit 0.2 % (content basis)
Show targets (13 of 13)
- Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
- Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
- Diethylamino Hydroxybenzoyl Hexyl Benzoate (DHHB) (Benzoic acid, 2-[4-(diethylamino)-2- hydroxybenzoyl]-, hexyl ester; CAS 302776-68-7)
- Citral Geranial (CAS 5392-40-5)
- Citral Geranial (CAS 5392-40-5)
- Citral Geranial (CAS 5392-40-5)
- Zinc Acetate (CAS 557-34-6)
- Acetylated Vetiveria Zizanioides Root Extract (Vetiveria zizanioides, ext., acetylated Oils, vetiver, acetylated; CAS 84082-84-8)
- Acetylated Vetiveria Zizanioides Root Extract (Vetiveria zizanioides, ext., acetylated Oils, vetiver, acetylated; CAS 84082-84-8)
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
Every product in the category
1 Jan 2027
Each rule has its own date; open a target.
Example: Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
From the consolidated text: (g) Face make-up and make-up remover products · (g) 0,2 %
Annex III entry 75 (l6) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)Limit 0.004 % (content basis)
In the finished (ready for use) cosmetic product. Maximum concentration cell: (h) 0,004 %. Field of application: (h) Oral 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.
- Applied to: Mouth or Teeth and gums
Depends on: body area
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: (h) Oral products · (h) 0,004 %
Annex III entry 75 (l7) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)- WarningUS-CAN-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-CABisphenol 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-CATacrolimus (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-CAHydrochlorothiazide
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-CAVoriconazole
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-CAWelding 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)
- BanEUTriphenyl 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
Annex II entry 1767 · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
- LimitEUBenzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
Limit 0.7 % (content basis)
In the finished (ready for use) cosmetic product. Maximum concentration cell: (f) 0,7 %. Field of application: (f) Body lotion.
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
- Applied to: Body
Depends on: body area
- 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: (f) Body lotion · (f) 0,7 %
Annex III entry 75 (l5) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
- Limit x 13EU
13 rules from Regulation (EC) No 1223/2009 on cosmetic products, Annexes II-VI (consolidated)
Limit 0.2 % (content basis)
Show targets (13 of 13)
- Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
- Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
- Diethylamino Hydroxybenzoyl Hexyl Benzoate (DHHB) (Benzoic acid, 2-[4-(diethylamino)-2- hydroxybenzoyl]-, hexyl ester; CAS 302776-68-7)
- Citral Geranial (CAS 5392-40-5)
- Citral Geranial (CAS 5392-40-5)
- Citral Geranial (CAS 5392-40-5)
- Zinc Acetate (CAS 557-34-6)
- Acetylated Vetiveria Zizanioides Root Extract (Vetiveria zizanioides, ext., acetylated Oils, vetiver, acetylated; CAS 84082-84-8)
- Acetylated Vetiveria Zizanioides Root Extract (Vetiveria zizanioides, ext., acetylated Oils, vetiver, acetylated; CAS 84082-84-8)
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
- Aluminium-containing ingredients with the exception of those listed in entries 34, 50, 189, 190 and 192 of Annex III, in entries 117, 118, 119, 121, 131, 150 of Annex IV, in entry 61 in Annex V, and entry 27a of Annex VI.
- Applies when
Every product in the category
- Effective
1 Jan 2027
Each rule has its own date; open a target.
- Source
Example: Benzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
From the consolidated text: (g) Face make-up and make-up remover products · (g) 0,2 %
Annex III entry 75 (l6) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
- LimitEUBenzyl Salicylate (2-hydroxybenzoic acid phenylmethyl ester; CAS 118-58-1)
Limit 0.004 % (content basis)
In the finished (ready for use) cosmetic product. Maximum concentration cell: (h) 0,004 %. Field of application: (h) Oral 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
- Applied to: Mouth or Teeth and gums
Depends on: body area
- 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: (h) Oral products · (h) 0,004 %
Annex III entry 75 (l7) · fetched 2026-10-09
European Commission / Publications Office (CELLAR): Reg. (EC) 1223/2009 Annexes II-VI(opens in a new tab)
Records
Recalls and alerts
Recalls, safety alerts and Prop 65 notices that name Deodorants and antiperspirants, with a link to the original. A Prop 65 notice is a claim by the sender, not a ruling.
300 records dated 17 Mar 2023 to 21 Aug 2026. Most recent shown.
Show the 8 most recent records
- Safety Gate alerts
Deodorant - men
Origin as stated: Germany
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
- Safety Gate alerts
Deodorant - D.E.O-Balm
Origin as stated: Austria
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
- Safety Gate alerts
Deodorant - PURE GAME
Origin as stated: France
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
- Safety Gate alerts
Deodorant - ISLAND VIBES
Origin as stated: Germany
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
- Safety Gate alerts
Deodorant - control
Origin as stated: Portugal
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
- Safety Gate alerts
Deodorant - Coral Dream
Origin as stated: France
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
- Safety Gate alerts
Deodorant - Blooming Sense
Origin as stated: France
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
- Safety Gate alerts
Deodorant - men Adventure ADRENALINE 48H
Origin as stated: United Kingdom
Cosmetics and personal care
- Substance
- None named
- Party
- Not stated
- Category
- Deodorants
Sub-categories
Further rules in sub-categories
These apply only to the sub-categories below, not to the whole category.
- Deodorants1 additional rule
See also
Related categories
- Cosmetics and personal care
Cosmetic products as defined in EU Reg. 1223/2009 Art. 2, FD&C Act sec. 201(i), the Korean Cosmetics Act and the Japanese PMD Act: substances or mixtures for external parts of the body, teeth or mucous membranes of the mouth, to clean, perfume, change appearance, protect, keep in good condition or correct body odours. Tattoo inks, drugs, devices and quasi-drug claims (JP/KR functional claims, US OTC drug claims) are flagged with attributes or claims, not separate roots.
- Deodorants
Cosmetic deodorants that mask or reduce odour without an antiperspirant claim.
- Antiperspirants
Products claiming to reduce perspiration (US: OTC drug, 21 CFR 350 monograph; EU/UK/KR/JP: cosmetic or functional).
- Skin care
Face and body skin products, sun protection and exfoliants.
- Hair care and colour
Shampoos, styling, waving, straightening and hair dyes.
- Nail products
Nail polish, care and artificial nail systems.
- Make-up
Colour cosmetics for face, eyes, lips and lashes.
- Oral care
Toothpaste, mouthwash and tooth whitening.
Alerts
Get an email when these rules change.
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