The US Food and Drug Administration has published a Structured Product Labeling (SPL) Implementation Guide with Validation Procedures. Cosmetic product facility registrations and product listings are now included within the SPL framework. The Implementation Guide can be used to develop SPL authoring tools. In the future, once FDA begins accepting data, users may transmit SPL-formatted submissions through FDA’s Electronic Submissions Gateway (ESG), or SPL authoring software including Xforms, for cosmetic product facility registrations and product listings, mandated by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA).

We have collected the latest FAQs on ordinary cosmetics filing from the Guangzhou Administration for Market Regulation and translated them into English for your reference.

We have collected the latest FAQs on ordinary cosmetics filing from the Guangzhou Administration for Market Regulation and translated them into English for your reference.

On September 22, 2023, the Scientific Committee on Consumer Safety (SCCS) issued a final opinion on methyl salicylate to assess its safety and use in cosmetics. In the SCCS/1633/21 Opinion, the Committee concluded that Methyl Salicylate (CAS No.119-36-8) in toothpaste is safe for children under six years of age when used up to the maximum concentration of 2.52%.

On August 2, 2023, the Indonesian Food and Drug Administration (Badan Pengawas Obat dan Makanan, BPOM) published Regulation No. 17 of 2023 on the Product Information File (PIF) guidelines for cosmetics, which came into effect from the date of publication. Parties that obtain product notification codes before August 2, must update PIF within six months. The PIF should be prepared by cosmetic manufacturers and importers and should be submitted to the BPOM before products obtain market authorization.

We have collected the latest FAQs on ordinary cosmetics filing from the Guangzhou Administration for Market Regulation and translated them into English for your reference.

On July 20, 2023, the United Kingdom issued the Cosmetic Products (Restriction of Chemical Substances) Regulations 2023 (No. 836 of 2023), to revise the requirements for the use of Methyl-N-methylanthranilate (CAS No. 85-91-6), HAA, and HAA (nano) (CAS No. 919803-06-8). This regulation applies to England, Wales, and Scotland.

The US FEI Portal allows a user to look up an FDA Establishment Identifier (FEI) based on a firm name and address, or validate the address of an FEI.

On August 7, 2023, the US Food and Drug Administration (FDA) published draft guidance on cosmetic product facility registrations and product listings, as mandated by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA). When finalized, the draft guidance will assist stakeholders with cosmetic product facility registration and product listing submissions to FDA, by describing who is responsible for making the registration and listing submissions, what information to include, how to submit, and when to submit, as well as certain exemptions to the registration and listing requirements.

We have collected the latest FAQ on the ordinary cosmetics filing from the Guangzhou Administration for Market Regulation and translated them into English for your reference.