EU Cosmetics Regulation is under review
Topic: EU COSMETICS REGULATION

Date of publication: 21/02/2025

On February 21 2025, the European Commission opened a Call for Evidence to assess the effectiveness of the Cosmetic Products Regulation. The revision is open for comments until March 21, 2025.

What’s new?

On February 21 2025, the European Commission opened a Call for Evidence to evaluate the effectiveness of the Cosmetic Products Regulation (CPR). This initiative aims to assess whether the current regulatory framework is achieving its primary objectives of protecting consumer health and ensuring the smooth functioning of the internal market across the European Union.

The evaluation will focus on five key elements: effectiveness in achieving objectives, efficiency including cost benefits, relevance in the current context, coherence with other EU chemical legislations (such as REACH and CLP Regulations), and the EU “added value” compared to national-level regulatory frameworks.

The European Commission has invited input from all interested stakeholders, including public authorities at national, regional, and local levels, businesses, civil society organisations, and individual citizens.

What now?

The Call for Evidence is open for comments until March 21, 2025. This represents the first phase of a broader evaluation process, with a public consultation expected to follow in May or June 2025, followed by a targeted consultation.

Commission adoption is expected for Second quarter 2026.

References:

Cosmetic Products Regulation – evaluation

other REGULATORY UPDATES

Regulation (EU) 2022/1531 – OMNIBUS ACT V – applicable as of 17 December 2022

Ingredients: METHYL SALICYLATE, SODIUM HYDROXYMETHYLGLYCINATE, DBMC, MIBK

Date of publication: 15/09/2022

Date of application: 17/12/2022

The European Commission has published the Commission Regulation (EU) 2022/1531, which amends the Regulation (EC) No 1223/2009 as regards the use in cosmetic products of certain substances classified as CMR, by adding new entries to Annex II and Annex III and revising an entry in Annex V.

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UK Responsible Person Labelling Deadline Extension

RESPONSIBLE PERSON

Date of application: 31/12/2025

The UK Office for Product Safety and Standards (OPSS) have reviewed the requirement to label the product with the UK Responsible Person and have decided to extend this transitional provision for a total period of five years, until 31 December 2025.

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SCCS Revision of the Scientific Opinion on Vitamin A

Ingredients: RETINOL, RETINYL PALMITATE, RETINYL ACETATE, RETINYL LINOLEATE, RETINAL

Date of publication: 25/10/2022

The Scientific Committee on Consumer Safety has issued a final version of the Scientific Opinion on Vitamin A, concluding that exposure to Vitamin A derived from cosmetics can be a concern for higher exposure consumers, and since cosmetics alone do not exceed the upper limit the SCCS cannot suggest maximum concentration limits that take into account contributions from other sources.

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Any REGULATORY QUESTION?

French Anti-Waste Law – Impact in Cosmetics Packaging and Labelling

PACKAGING WASTE MANAGEMENT

Date of application: 01/01/2023, with a transition period until 09/03/2023 for packaging produced or imported before 09/09/2022.

The Loi relative à la lute contre le gaspillage et a l’économie circulaire (Anti-Waste for a circular economy) has come officially into force in France in 2020. From January 2023 the requirements of the law became mandatory, including specific symbols on the packaging or labelling of cosmetic products.

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SCCS Final Opinion on the Safety of Triclocarban and Triclosan

Ingredients: TRICLOCARBAN and TRICLOSAN

Date of publication: 25/10/2022

During the plenary meeting on 24-25 October 2022, the Scientific Committee on Consumer Safety (SCCS) presented its final opinion on the safety of Triclocarban and Triclosan as substances with potential endocrine disrupting properties in cosmetic products.

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