Author name: Cosmereg

Bill 96 Cosmetics Canada

Canada Cosmetic Regulations / By

Québec’s Bill 96 introduces strict French-language requirements for cosmetic brands selling in the province. From product labels to websites and customer service, brands must ensure French is clearly and equally displayed across all consumer touchpoints. This includes translating ingredient lists, marketing claims, and even parts of registered trademarks by 2025. Failure to comply can lead to fines, product removal, or reputational damage. In this guide, we explain how Bill 96 affects cosmetics, what changes are mandatory, and what steps brands must take to remain compliant in the Québec market.

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Understanding the Difference Between Shelf Life and PAO in EU Cosmetic Regulation

EU Cosmetic Regulations / By

When selling cosmetic products in the European Union, understanding the difference between shelf life and Period After Opening (PAO) is crucial for regulatory compliance. This article explains these two concepts as defined by EU Cosmetic Regulation (EC) No 1223/2009, including when to use each, what documentation is required, and how to remain compliant.

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Key Developments in EU and UK Regulations: Early 2023 Updates

Amazon Dietary Supplements Requirements USA

US FDA Dietary Supplements / By

Navigating Amazon Dietary Supplements Requirements: A 2025 Compliance Guide Selling dietary supplements on Amazon USA can be highly profitable, but it also involves strict compliance with both Amazon’s internal policies and U.S. federal regulations. In recent years, Amazon has significantly tightened its oversight on supplement listings, making it critical for sellers—both domestic and international—to understand

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FDA Cosmetic Registration & MoCRA Listing | Cosmereg

USA Cosmetic Regulations / By

FDA Cosmetic Registration: MoCRA Product Listing Requirements Understanding FDA Cosmetic Registration and MoCRA Obligations FDA cosmetic registration is now a requirement under the Modernization of Cosmetics Regulation Act (MoCRA), signed into law in December 2022. This regulation introduces mandatory listing obligations for all cosmetic products marketed in the United States. Every cosmetic item must be

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FDA Proposes Mandatory Asbestos Testing for Talc-Based Cosmetics: What It Means for Industry Compliance

USA Cosmetic Regulations / By

FDA Proposes Mandatory Asbestos Testing for Talc-Based Cosmetics: What It Means for Industry Compliance Overview On March 25, 2025, the U.S. Food and Drug Administration (FDA) proposed a long-anticipated rule requiring mandatory, standardized testing for asbestos in talc-based cosmetic products. This move is a direct response to consumer safety concerns and past reports of asbestos

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Export Food & Dietary Supplements to the USA | FDA Registration & US Agent Service

US FDA Dietary Supplements, US FDA food regulations / By

How to Export Food and Dietary Supplements to the USA: Understanding FDA Facility Registration and the Role of a US Agent The Importance of Facility Registration and a US Agent Exporting food and dietary supplements to the United States is a significant opportunity for international businesses, given the high demand for quality food and health

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Adverse Event Reporting for Cosmetics | MOCRA Compliance with Cosmereg

Adverse Event Reporting for Cosmetics | MOCRA Compliance with Cosmereg

US FDA Dietary Supplements, US FDA food regulations, US FDA Medical Devices, US FDA OTC regulations, USA Cosmetic Regulations / By

What is Adverse Event Reporting for Cosmetic Products? | MOCRA Compliance with Cosmereg With the Modernization of Cosmetics Regulation Act of 2022 (MOCRA), the U.S. FDA has strengthened regulatory requirements for cosmetic products, bringing them closer to the standards seen in food and drug industries. One of the most significant changes is the mandatory reporting

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UK Implements Ban on 64 Harmful Substances and Limits Kojic Acid in Cosmetics

UK Cosmetic Regulations / By

UK Implements Ban on 64 Harmful Substances and Limits Kojic Acid in Cosmetics   On December 17, 2024, the UK government announced new cosmetic safety regulations under Statutory Instrument 2024 No. 1334. These changes include banning 64 substances classified as Carcinogenic, Mutagenic, or Reprotoxic (CMR) and imposing stricter rules on the use of kojic acid,

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