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USA Cosmetic Regulations

FDA Draft Guidance on Mandatory Cosmetic Recalls Under MoCRA: What Brands Must Know

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FDA Draft Guidance on Mandatory Cosmetic Recalls Under MoCRA: What Brands Must Know On 18 December 2025, the U.S. Food and Drug Administration announced the availability of a new draft guidance document titled “Questions and Answers Regarding Mandatory Cosmetics Recalls: Guidance for Industry.”This guidance represents a critical enforcement clarification under the Modernization of Cosmetics Regulation […]

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Proposition 65 titanium dioxide

California Prop 65: Safe Harbor Levels for Titanium Dioxide

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California Adopts Proposition 65 Safe Harbor Levels for Titanium Dioxide California has officially established Safe Harbor exposure limits for titanium dioxide (airborne, unbound particles of respirable size) under Proposition 65 — the state’s law requiring businesses to warn consumers about potential exposure to chemicals linked to cancer or reproductive harm. New Safe Harbor Limits According

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California SB 236 Hair Relaxer Bill – What Cosmetic Brands Must Know

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California SB 236 Hair Relaxer Bill: What It Means for Cosmetic Brands California has once again taken the lead in cosmetic safety with the introduction of SB 236, the Hair Relaxer Bill (C.U.R.L. Act). This new law is set to reshape how hair relaxer products are formulated, tested, and sold in California. If your brand

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FDA FAERS Public Dashboard for Cosmetic Products

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  FDA Launches FAERS Public Dashboard for Cosmetic Products: Transparency in Adverse Event Reporting On September 12, 2025, the U.S. Food and Drug Administration (FDA) introduced the FAERS Public Dashboard for Cosmetic Products, a new interactive platform designed to improve cosmetic safety monitoring and transparency. This tool gives real-time access to adverse event reports related

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Life After “De Minimis”: What Importers of Cosmetics, Food, and Supplements Must Know

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

Life After “De Minimis”: What Importers of Cosmetics, Food, and Supplements Must Know Introduction The elimination of de minimis import rules 2025 marks a turning point for global trade. The change rescinds previous rules allowing sub-$800. Shipments that once bypassed duties and simplified entry now require full customs clearance and compliance. For businesses importing cosmetics,

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How U.S. Tariffs Affect Imports of FDA-Regulated Products: What Importers Need to Know

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

How U.S. Tariffs Affect Imports of FDA-Regulated Products: What Importers Need to Know Introduction Importing FDA-regulated products into the U.S. involves more than just regulatory compliance. Rising U.S. tariffs on specific goods can significantly affect your business strategy, especially if you’re importing cosmetics, dietary supplements, food, or medical devices. This article explores how tariffs and

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FDA Cosmetic Registration & MoCRA Listing | Cosmereg

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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

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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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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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Washington State Toxic-Free Cosmetics Act

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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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