Understanding the FDA’s cosmetic labeling requirements is crucial for ensuring that products are legally compliant and safe for consumers. The Federal Food, Drug, and Cosmetic Act mandates specific labeling protocols to prevent misbranding and misinformation. Key elements required on the principal display panel include the product’s identity and the net quantity of contents. The identity must clearly indicate the nature of the cosmetic product, while the net quantity must be expressed in both metric and customary units. Additionally, the information panel must display an ingredient list in descending order of predominance, ensuring transparency and enabling consumers to make informed choices.
Accurate and clear labeling serves not only to comply with regulatory standards but also to build consumer trust and brand integrity. The FDA also requires that the label includes the name and place of business of the manufacturer, packer, or distributor, as well as any relevant warnings and directions for safe use. Labels must be prominently placed and easily legible, with all required information in English, unless the product is marketed solely in a territory where another language is predominant. Non-compliance can result in severe consequences, including product recalls, legal action, and damage to the brand’s reputation. Therefore, adhering to FDA cosmetic labeling requirements is essential for market access and consumer safety.FDA Cosmetic Labeling Requirments