Ingrédient

ÉTATS-UNIS

Benchmarking the EU: Illinois Passes Legislation Banning 12 Categories of Cosmetic Ingredients

On July 10, 2026, the State of Illinois officially enacted the Chemicals in Cosmetic Products Act. The legislation aims to align state standards with prohibitions established under EU Regulation (EC) No 1223/2009 and its subsequent amendments regarding intentionally added chemical ingredients in cosmetics, signaling a growing trend toward global convergence in cosmetic safety regulation. Core Provisions of the Act Beginning July 1, 2028, except under specified circumstances, no entity or individual may manufacture, transport, store, or sell cosmetic products within the State of Illinois containing any of the following intentionally added ingredients: Exemption Criteria The act establishes a specific trace impurity exemption: if a cosmetic product is manufactured using processes designed to comply with the legislation, the presence of technically unavoidable trace amounts resulting from impurities in natural or synthetic ingredients, manufacturing processes, storage, or primary packaging shall not constitute a violation. Industry Impact and Outlook The passage of the

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Brésil

Brazil ANVISA Issues New Cosmetics Regulations: Updated Prohibited and Restricted Ingredient Lists

On June 11, 2026, the Brazilian Health Regulatory Agency (ANVISA) approved two technical resolutions—RDC No. 1,029/2026 and RDC No. 1,030/2026—significantly updating ingredient compliance for personal hygiene products, cosmetics, and perfumes. Officially published in the Diário Oficial da União (DOU) on June 15, 2026, these regulations internalize Southern Common Market (MERCOSUR) resolutions to align regional safety standards. Below is an overview of the regulatory changes, specific chemical impacts, transition timelines, and actionable steps for brand owners, exporters, and ingredient manufacturers. Key Regulatory Highlights 1. RDC No. 1,030/2026 — Updated Prohibited Substances List Amending the annex of RDC No. 529/2021, this resolution incorporates MERCOSUR GMC Resolution No. 07/25 to expand and refine the list of banned substances. 2. RDC No. 1,029/2026 — Updated Restricted Substances List This resolution revokes and replaces RDC No. 530/2021, internalizing MERCOSUR GMC Resolution No. 06/25. It establishes mandatory conditions, maximum allowed concentrations, and required label warnings. Implementation

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L'UE

EU Notifies WTO of Draft Cosmetics Regulation Revision: Total Ban on Mercury, Strict Limits Introduced for CBD and BHA

On July 8, 2026, the European Commission notified the World Trade Organization (WTO) of a draft regulation amending Regulation (EC) No 1223/2009 on cosmetic products. The draft was developed in reference to the new classification of Carcinogenic, Mutagenic, or Reprotoxic (CMR) substances introduced under Commission Delegated Regulation (EU) 2025/1222, as well as the latest scientific evaluation results released by the Scientific Committee on Consumer Safety (SCCS) between 2025 and 2026. The public comment period runs through September 6, 2026, with adoption expected in the fourth quarter of 2026. Revisions and Additions to Annex II (List of Prohibited Substances) Revisions and Additions to Annex III (List of Restricted Substances) 1. Revision of Permitted Conditions and Restrictions for Hydroxyapatite (nano): Permitted Product Types and Maximum Concentration in Cosmetics Other Restrictions Hydroxyapatite (nano)(a) Toothpaste: 29.5%(b) Mouthwash: 10% For items (a) and (b):– Shall not be used in applications that may lead to exposure

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ANASE

2026 ASEAN Cosmetic Directive (ACD) Annex Updates: Major Restrictions and Bans Enforced for Kojic Acid, Preservatives, and Other Ingredients

The ASEAN Cosmetic Directive (ACD) is a regional agreement designed to harmonize technical requirements for cosmetic products across ASEAN member states, eliminating technical barriers to trade and facilitating free market circulation. The ASEAN Cosmetic Committee (ACC) and the ASEAN Cosmetic Scientific Body (ACSB) convene biannually to review and update regulatory standards. On June 30, 2026, official revisions were promulgated for Annex II (Prohibited Substances), Annex III (Restricted Substances), Annex IV (Allowed Colorants), and Annex VI (Allowed Preservatives). I. Annex II — Prohibited Substances List Key updates to the prohibited list involve newly added antifungal agents, tightened thresholds for hazardous impurities, and item adjustments: (Note: The four substances added above are antifungal ingredients commonly used in pharmaceuticals and are now explicitly banned from cosmetic formulations across ASEAN.) II. Annex III — Restricted Substances List Revisions to the restricted list directly alter maximum concentration limits for formulations, with significant restrictions placed on

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Close-up of SPF 60 UV protection cream for skincare, featuring floral accents and a natural setting.
ÉTATS-UNIS

La FDA approuve officiellement le bémotrizinol, un ingrédient de crème solaire de nouvelle génération : une nouvelle ère pour la protection solaire américaine commence

Le 10 juin 2026, l’Agence américaine des produits alimentaires et médicamenteux (FDA) a rendu une décision réglementaire historique : l’arrêté administratif définitif OTC000039. Cet arrêté modifie officiellement la monographie M020 relative aux produits solaires en vente libre (OTC) M020 afin d’autoriser l’utilisation d’un tout nouvel ingrédient actif, le bemotrizinol (bis-éthylhexyloxyphénol méthoxyphényl triazine), dans les crèmes solaires en vente libre à une concentration maximale autorisée de 6%. C’est la première fois en plus de deux décennies qu’un filtre UV chimique véritablement moderne et innovant est ajouté à la monographie américaine sur les produits solaires, ce qui marque une étape décisive pour le marché américain des soins solaires. I. Qu’a déclaré la FDA ? Selon l’arrêté administratif final exhaustif de 35 pages, la FDA a examiné de manière approfondie les nombreuses données scientifiques relatives à la sécurité ainsi que les commentaires du public soumis par le fabricant à l’origine de la demande, DSM Nutritional Products. L’agence a officiellement conclu que le bemotrizinol est « généralement reconnu comme sûr et efficace » (GRASE) pour une utilisation en tant qu’ingrédient actif de protection solaire à des concentrations allant jusqu’à 6%. II. Deux fondements essentiels

La FDA approuve officiellement le bémotrizinol, un ingrédient de crème solaire de nouvelle génération : une nouvelle ère pour la protection solaire américaine commence Lire la suite »