Tag: cosmetic regulatory compliance
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Cosmetic Labeling Requirements Under US FDA: Compliance Framework for Cosmetic Brands
Cosmetic labeling is not just a marketing activity—it is a legal obligation under United States law. Every cosmetic product sold in the US must carry labeling that is truthful, not misleading, and compliant with regulations enforced by the US FDA. With the implementation of the Modernization of Cosmetics Regulation Act (MoCRA), labeling compliance has become…
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How to Get an FEI Number: Complete Guide for Cosmetic Facilities
The FDA Establishment Identifier (FEI) is a unique number assigned by the US FDA to identify facilities that manufacture, process, pack, or hold regulated products, including cosmetics. Under the Modernization of Cosmetics Regulation Act (MoCRA), facility identification and traceability have become central to cosmetic regulatory compliance, making FEI numbers increasingly important for cosmetic manufacturers and…
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Cosmetic Product Safety Substantiation: Building Scientific Proof of Safety Under MoCRA
Cosmetic safety in the United States is no longer based on informal assurances or internal opinions. With the enactment of the Modernization of Cosmetics Regulation Act (MoCRA), cosmetic companies are now legally required to maintain adequate safety substantiation for every cosmetic product marketed in the United States. Under the authority of the US FDA, cosmetic…
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Cosmetic Product Safety Substantiation: Building Scientific Proof of Safety Under MoCRA
Cosmetic safety in the United States is no longer based on informal assurances or internal opinions. With the enactment of the Modernization of Cosmetics Regulation Act (MoCRA), cosmetic companies are now legally required to maintain adequate safety substantiation for every cosmetic product marketed in the United States. Under the authority of the US FDA, cosmetic…
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US FDA Mandatory Cosmetic GMP: What MoCRA Means for Cosmetic Manufacturing Compliance
The regulatory expectations for cosmetic manufacturing in the United States have changed dramatically with the passage of the Modernization of Cosmetics Regulation Act (MoCRA). One of the most important outcomes of MoCRA is the clear movement toward mandatory Cosmetic Good Manufacturing Practices (GMP) under the authority of the US FDA. While cosmetic GMP was historically…
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Cosmetic Good Manufacturing Practices (GMP): Building Compliance Under US FDA and MoCRA
In today’s regulatory environment, product safety begins long before a cosmetic reaches the shelf. It starts inside the manufacturing facility. Cosmetic Good Manufacturing Practices (GMP) are the operational foundation that ensures products are consistently produced and controlled according to quality standards. Under the authority of the US FDA, and reinforced by the Modernization of Cosmetics…
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PFAS in Cosmetics: US FDA Regulatory Expectations and MoCRA Compliance Strategy
Per- and polyfluoroalkyl substances (PFAS) have become one of the most scrutinized chemical groups in consumer products, including cosmetics. Often referred to as “forever chemicals,” PFAS are valued for their water-resistant, oil-resistant, and long-lasting properties. However, concerns about persistence in the environment and potential health risks have drawn increased regulatory attention. Under the authority of…
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Asbestos in Talc Cosmetics: US FDA Regulatory Expectations and Compliance Strategy
Talc has long been used in cosmetic products such as face powders, body powders, and certain pressed makeup formulations. However, concerns regarding asbestos contamination in talc have significantly increased regulatory scrutiny in recent years. Under the authority of the US FDA and strengthened by the Modernization of Cosmetics Regulation Act (MoCRA), cosmetic manufacturers must ensure…