Tag: US FDA consultancy
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Modernization of Cosmetics Regulation Act of 2022 (MoCRA): Comprehensive Compliance Guide for Cosmetic Brands
In December 2022, the United States enacted a landmark law that fundamentally reshaped cosmetic regulation—the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). This legislation represents the most significant update to cosmetic law in over 80 years and dramatically expanded US FDA authority over cosmetic products marketed in the United States. Before MoCRA, cosmetic regulation…
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Fair Packaging and Labeling Act (FPLA) and Cosmetics: How US Law Controls Cosmetic Label Transparency
In the United States, cosmetic labels are more than marketing tools—they are legal documents. Every word, number, and claim appearing on cosmetic packaging is regulated under federal law. One of the most important statutes governing this area is the Fair Packaging and Labeling Act (FPLA). The FPLA works alongside the Federal Food, Drug, and Cosmetic…
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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…
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US Cosmetic Law: Regulatory Foundations, Modern Compliance Obligations, and Strategic Pathways for Cosmetic Brands
Entering or expanding within the United States cosmetic market requires more than innovative formulations and attractive packaging. Every cosmetic product sold in the US must align with a complex legal framework designed to protect consumer safety and ensure market transparency. US Cosmetic Law establishes the legal backbone governing how cosmetics are manufactured, labeled, distributed, and…