Tag: What are the FDA regulations for cosmetics?
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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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Serious Adverse Event Reporting for Cosmetics: US FDA MoCRA Compliance Explained
The Modernization of Cosmetics Regulation Act (MoCRA) has significantly strengthened post-market safety oversight for cosmetic products in the United States. One of the most critical obligations introduced under MoCRA is mandatory serious adverse event reporting to the US FDA. Cosmetic companies are now legally required to report serious adverse events associated with their products within…
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Federal Food, Drug, and Cosmetic Act (FD&C Act) and Cosmetics: The Legal Backbone of US Cosmetic Regulation
The United States cosmetic industry operates under a powerful federal law that shapes how products are manufactured, labeled, marketed, and monitored. The Federal Food, Drug, and Cosmetic Act (FD&C Act) forms the foundation of cosmetic regulation in the United States and establishes the authority of the US FDA over cosmetic products. Every cosmetic brand—whether domestic…