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 […]
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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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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FDA Cosmetic Labeling guide, Why is it so important? The cosmetics sold in the USA must comply with the labeling regulations published by the FDA. As FDA cosmetic labeling is not only used to help inform consumers of a product’s intended use and any related warnings, also notify its ingredients, the net quantity of contents,
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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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New EU Rules on Triclocarban and Triclosan in Cosmetics The European Union is stepping up its safety measures for cosmetics. From 31 December 2024, new rules under Regulation (EU) 2024/996 will limit how much Triclocarban and Triclosan can be used in cosmetic products. Any existing products on store shelves must meet these rules by 31
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Navigating the Washington State Toxic-Free Cosmetics Act: What Cosmetic Manufacturers Need to Know The Washington State Toxic-Free Cosmetics Act represents a significant step forward in protecting consumers from potentially harmful chemicals in personal care products. This legislation places a strong emphasis on ingredient safety and transparency, requiring cosmetic manufacturers and importers to comply with stricter
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FDA Bans Red Dye No. 3 in Foods and Drugs: What This Means for Manufacturers and Consumers In a landmark decision announced earlier this week, the U.S. Food and Drug Administration (FDA) declared a ban on the use of Red Dye No. 3 (FD&C Red No. 3) in foods and orally ingested drugs. The decision
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MoCRAÂ Allergen Labeling Delays: What You Need to Know The Modernization of Cosmetics Regulation Act (MoCRA), passed in December 2022, is shaking up the cosmetics industry in the United States. This law brings big changes, including clearer allergen labeling requirements. However, recent updates from the FDA have pushed back the timelines: Allergen Labeling
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PFAS in Cosmetics: Understanding the Regulatory and Consumer Landscape in the United States In recent years, the presence of Per- and Polyfluoroalkyl Substances (PFAS) in cosmetics has sparked significant concern among consumers, regulators, and industry professionals in the United States. Commonly referred to as “forever chemicals” due to their persistence in the environment and
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