药品标签审核

《食品、药品和化妆品法》（FD&C）和《公平包装和标签法》（FPLA）授权FDA管理化妆品标签。本规定旨在告知客户产品的预期用途、警告、成分、净含量以及制造商、包装商或经销商的信息。它们还保护客户免受危害，并禁止虚假或误导性信息。

Drug Product Label Review

We helps drug customers to comply with FDA labeling regulations and assist with labeling preparation. The regulations are intended to inform the customers of the product's intended use, warning, ingredients, net quantity of contents, and information of manufacturer, packer or distributor. They also protect customers from hazards, and prohibit against false or misleading information.