US FDA Approves Bemotrizinol as New Sunscreen Active Ingredient Under OTC Monograph M020
What is the FDA approval of bemotrizinol and why does it matter? The FDA approved bemotrizinol (BEMT) as a new over the counter (OTC) sunscreen active ingredient in June 2026, marking the first new sunscreen filter added to the U.S. monograph system in over 20 years. The broad-spectrum, photostable UV filter provides UVA/UVB protection, is […]
Washington Recycling Reform Act: Packaging EPR Rulemaking Updates
What do businesses need to know about Washington’s Recycling Reform Act and packaging EPR rollout? Washington is advancing its packaging EPR program through the Recycling Reform Act rulemaking process, with new rules expected to define producer registration, PRO responsibilities, reporting, fees, and reimbursements. The program will shift packaging waste costs to producers, with implementation planning […]
Maryland Senate Bill 901: EPR Implementation Updates for Packaging and Paper Products
What do businesses need to know about Maryland Senate Bill 901’s packaging EPR implementation? Maryland’s packaging EPR program is advancing with new regulations establishing producer registration requirements, Circular Action Alliance appointed as the PRO, and future rules expected to clarify reporting requirements, fees, performance targets, and producer obligations. When did Maryland’s Senate Bill 901 packaging […]
California SB 54 Packaging EPR: Stakeholder Reports Due May 31 Will Shape Future Fees
How will California’s SB 54 packaging EPR stakeholder reports shape future producer fees? California’s May 31 SB 54 packaging EPR stakeholder reports will help shape future producer fees by providing data on packaging materials, recycling performance, collection systems, and market conditions. When was the deadline for California’s SB 54 EPR stakeholder reports? California’s packaging Extended […]
Safety Alert: US Nail Polish Remover Recall Highlights Risks of Prohibited Solvents
A recent enforcement action in the United States has led to the high-profile recall of nail polish remover products following the detection of methylene chloride and chloroform. Both substances are strictly prohibited in cosmetic formulations globally due to their significant health risks. Methylene chloride and chloroform are volatile organic compounds recognized for their hazardous profiles, […]
What are the main differences between EU and U.S. INCI list rules after MoCRA?
EU INCI rules require greater ingredient transparency, including allergens, colorants, and nanomaterials. MoCRA strengthens U.S. oversight through product listing, facility registration, and post-market controls. As a result, global cosmetic companies must manage INCI lists as part of a broader compliance strategy. INCI List Differences Between EU and U.S.: Why Understanding Matters The comparison of ingredient […]
What are MoCRA requirements for cosmetic brands?
MoCRA requirements introduce mandatory U.S. regulations for cosmetics, including facility registration, product listing, safety substantiation, and adverse event reporting. They apply to both domestic and international brands, enhancing consumer safety, traceability, and regulatory accountability. Understanding and implementing these requirements is essential to maintain market access and stay compliant. MoCRA Requirements: A Structural Shift in U.S. […]
What Is MoCRA Enforcement?
MoCRA reshapes U.S. cosmetics regulation by giving the FDA new authority and requiring mandatory compliance, including facility registration, product listing, safety substantiation, and adverse event reporting for both domestic and international brands, while enhancing consumer protection, traceability, and brand accountability. MoCRA Enforcement: A New Era in U.S. Cosmetic Oversight MoCRA has reshaped the U.S. cosmetics […]