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 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 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 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 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 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
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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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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MoCRA 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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MOCRA Cosmetics Labeling Requirements Introduction to MOCRA Cosmetics Labeling Requirements in the United States Cosmetic products marketed in the United States must comply with strict labeling requirements outlined by the U.S. Food and Drug Administration (FDA). Proper labeling ensures that products are not misbranded or misleading, and that consumers can make informed purchasing decisions.
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