As the US Food and Drug Administration (FDA) is about to issueCosmetics & Personal Carethe final guidelines for factory registration and product listing, the industrys attention continues to rise. The following is a summary of the latest progress:
FDA已于2023年8月放出了化妆品工厂注册和产品列名的指南草案,至今已吸引超过40条意见和建议。这些反馈涵盖了多方面的关注点,FDA正对这些建议进行评估,并将基于此发布最终指南。最终的发布意味着企业将获得更明确的方向,以便完成工厂注册和产品列名的要求。
In October this year, the FDA introduced the Structured Product Labeling (SPL) guidelines related to cosmetics. The use of SPL documents makes the information more standardized, facilitating the automatic processing of the FDAs database, and thus enabling timely and efficient updates of factory registration and product listing. The FDA has confirmed that in the near future, a new reporting system will be launched, and the specific start date will be announced in the next few weeks.
Enterprises should closely follow the updates regarding the launch of the electronic platform or the templates for submitting paper materials (Forms FDA 5066 and 5067). Although the FDA does not require the upload of SPL documents in the electronic system, and enterprises can also directly fill in the relevant information online, the standardized SPL documents are still the recommended option. For the traditional mode, the FDA still accepts the submission of paper materials.
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