Per- and polyfluoroalkyl substances (PFAS) are increasingly becoming a focal point of global concern due to their potential long-term impacts on the environment and human health. As a class of synthetic chemicals characterized by high stability and widespread applications, PFAS are facing increasingly stringent regulatory scrutiny in the cosmetics sector. This article explores the physicochemical properties and potential health risks of PFAS, and systematically reviews the evolving global regulatory landscape related to their use in cosmetics. It aims to help cosmetic enterprises gain a comprehensive understanding of regulatory requirements, mitigate compliance risks, enhance product safety, and strengthen competitiveness in international markets.

On November 20, 2025, the Department of Chemicals and Petrochemicals (DCPC) under the Ministry of Chemicals and Fertilizers of India issued multiple notifications announcing the withdrawal of six previously issued Quality Control Orders. This decision was made by the DCPC based on public interest considerations and in consultation with the Bureau of Indian Standards, in accordance with Section 16 of the Bureau of Indian Standards Act, 2016. The withdrawal took effect immediately upon announcement. Compliance actions already completed or initiated prior to the withdrawal remain unaffected.

On November 24, 2025, the Taiwan Food and Drug Administration (TFDA) under the Ministry of Health and Welfare officially issued the testing method for Sudan dyes in cosmetics (Method No. RA03D015.001), which came into effect upon the date of publication.

On November 21, 2025, the Official Journal of the European Union published three Commission Delegated Directives, introducing centralized revisions to multiple lead-related exemptions under the Restriction of Hazardous Substances (RoHS 2) Directive (2011/65/EU). These amendments focus on lead applications in alloys, glass/ceramics, and high melting temperature solders.