The FD&C Act prohibits the marketing of adulterated or misbranded cosmetics in interstate commerce. Violations of the Act involving product composition–whether they result from ingredients, contaminants, processing, packaging, or shipping and handling–cause cosmetics to be adulterated and subject to regulatory action. VTI can help you ensure that your processes, facilities, equipment and procedures adhere to GMP requirements (21 CFR parts FD&C) and are validated according to regulatory (FDA) standards.