Tag: fda mocra
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Cosmetics Direct: US FDA’s Centralized Platform for Cosmetic Regulatory Compliance
The Modernization of Cosmetics Regulation Act (MoCRA) has transformed how cosmetic products are regulated in the United States. To support these changes, the US FDA introduced a centralized electronic submission system known as Cosmetics Direct. This platform is designed to receive, manage, and process cosmetic regulatory submissions required under MoCRA. Cosmetics Direct serves as the…
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Responsible Person for Cosmetics Under US FDA: Legal Role, Duties, and Compliance Requirements
The Modernization of Cosmetics Regulation Act (MoCRA) introduced a major structural change in how cosmetic products are regulated in the United States. One of the most important concepts established under MoCRA is the designation of a Responsible Person for cosmetic products. The Responsible Person is the legally accountable party for ensuring that each cosmetic product…
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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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FDA MoCRA Cosmetic Registration: Complete Compliance Guide for Cosmetic Brands | XPRO America
The U.S. cosmetic regulatory landscape has undergone the most significant transformation in decades with the implementation of the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). For cosmetic manufacturers, brand owners, private-label companies, and foreign exporters targeting the United States market, FDA MoCRA Cosmetic Registration is no longer optional—it is a legal requirement. This article explains MoCRA in…