Tag: XPRO America
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Net Quantity of Contents on Cosmetic Labels: US FDA Requirements Explained
The net quantity of contents statement is one of the most fundamental and strictly enforced cosmetic labeling requirements in the United States. It tells consumers exactly how much product they are purchasing and allows fair comparison between products. Under the authority of the US FDA, and reinforced by the Modernization of Cosmetics Regulation Act (MoCRA),…
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Statement of Identity for Cosmetics: US FDA Labeling Requirement Explained
Every cosmetic product sold in the United States must clearly tell consumers what the product is. This simple concept is known in regulatory terms as the Statement of Identity. The Statement of Identity is one of the most fundamental labeling requirements enforced by the US FDA, and it appears on the cosmetic’s Principal Display Panel…
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Adulterated Cosmetics: Understanding US FDA Enforcement and MoCRA Compliance
Under United States law, cosmetic products must be safe for consumers under their intended conditions of use. When a cosmetic fails to meet safety or manufacturing standards, it may be classified as adulterated. An adulterated cosmetic is illegal to distribute in the United States and may trigger enforcement action by the US FDA. With the…
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Misbranded Cosmetics: How US FDA Defines, Detects, and Enforces Violations
Under United States law, cosmetic products must be labeled and marketed in a truthful, accurate, and non-misleading manner. When a cosmetic fails to meet these legal standards, it is considered misbranded. A misbranded cosmetic is illegal to distribute in the United States and may trigger enforcement action by the US FDA. With the implementation of…
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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…