Introduction to FDA Classification of Cosmetics U.S. FDA registered Cosmetics is a broad field that encompasses a variety of beauty and body care products. In order to ensure the health and safety of consumers, the U.S. Food and Drug Administration (FDA) has strict classification and regulation of cosmetics. These classifications are primarily based on the degree of risk and use of the product to ensure that only products that meet safety standards are able to enter the market. For more information, please visit the homepage.
Cosmetics FDA Registration and Certification Distinction Details The FDA's supervision of cosmetics is not limited to imports, but also includes products produced and sold domestically. All cosmetics sold in the U.S. must go through the FDA's registration and certification process. This process ensures the safety of the product's ingredients, the accuracy of the label, and the compliance of the product. FDA works closely with U.S. Customs and Border Protection (CBP) to monitor imported cosmetics. This means that any cosmetic products entering the U.S. must be inspected by CBP. This process is to prevent counterfeit, adulterated, or mislabeled products from entering the market. CBP may be denied entry into the U.S. if it finds any cosmetics that appear problematic or may pose a risk to public health. These products must either be processed for compliance or destroyed or re-exported. In addition, the FDA regularly publishes a list of cosmetic products that have been denied import on its ** and updates it monthly. Overall, FDA regulation of cosmetics is a multi-layered process designed to ensure that products used by U.S. consumers are safe and effective. By partnering with agencies such as CBP, the FDA is better able to fulfill its role to protect the public from substandard cosmetics. 
Do all imported cosmetics need to be sampled?The answer to this question is not absolute. In fact, not all imported cosmetics will be inspected or sampled upon entry into the country. In an effort to conduct inspections more efficiently, the U.S. Food and Drug Administration (FDA) has issued an import alert. This alert is meant to inform inspectors of non-compliance trends so that they can focus on those products that may be problematic. The products covered by the Import Alert include those cosmetic products that claim to have the best possible effect. These products may be considered new drugs that have not been approved by law, or cosmetics that have been adulterated due to microbial contamination. In addition, high-risk cattle tissues that do not meet U.S. requirements for color additives, as well as bulk shipments from countries with bovine spongiform encephalopathy (BSE), are also under the import alert. While the inspection of imported cosmetics is not limited to the types of products specified in the import alert, this alert provides an important reference for inspectors. At the same time, if a product appears to have violated U.S. law, the fact that it has not been previously seized does not protect the product from future seizure. While not all imported cosmetics are inspected upon entry, all imported cosmetics must comply with all legal requirements of the laws enforced in the United States. This includes products that have not been sampled for inspection, which also need to comply with relevant regulations or risk being seized or returned. As a result, importers and manufacturers need to conduct adequate compliance checks on the cosmetics they sell and produce to ensure compliance with all relevant regulations and standards. 