On December 15, 2023, the Scientific Committee on Consumer Safety (SCCS) of the European Union issued a final opinion on Methylparaben. The preliminary opinion on the safety of Methylparaben in cosmetics (SCCS/1652/23) was released on June 8, 2023.

On December 5, 2023, the European Union Scientific Committee on Consumer Safety (SCCS) published the preliminary opinion(SCCS/1661/23) on Titanium Dioxide (TiO2). The deadline for comments is set for 6 February 2024.

On December 14, 2023, the Taiwanese Ministry of Health and Welfare published a notice on the draft amendment of the List of Ingredients Prohibited in Cosmetic Products to commence a period of public comments. The new amendment will come into effect on July 1, 2024. For any comments or suggestions, please submit them within 60 days from the day following the publication of the notice.

FDA Direct is a U.S. Food and Drug Administration's web-based and free structured product labeling (SPL) authoring tool. Previously CDER Direct, FDA Direct now includes CDER Direct and Cosmetics Direct. Users can create separate accounts, depending on drugs or cosmetics submissions, or a single account that includes both CDER Direct submissions as well as Cosmetics Direct submissions.

Since the implementation of CSAR, according to data from the National Medical Products Administration (NMPA), as shown in Figure 1, in 2021, 6 new cosmetic ingredients obtained NMPA numbers, of which 4 were for domestically produced new cosmetic ingredients and 2 for imported cosmetic ingredients. In 2022, 42 new cosmetic ingredients obtained NMPA numbers, with 25 being domestically produced and 17 being imported. As of December 15, 2023, 60 new cosmetic ingredients have obtained NMPA numbers, with 46 being domestically produced and 14 being imported.

Since the publication of the Cosmetics Supervision and Administration Regulations (CSAR, State Order No. 727) on June 29, 2020, a series of supporting regulations have also been introduced. Included among all the supporting regulations are those relating to the registration and filing of new cosmetic ingredients in China, namely the: Measures for the Administration of Cosmetic Registration and Filing; Provisions on the Administration of New Cosmetic Ingredients Registration (hereafter the Provisions); and Filing Data and Technical Guidelines for Cosmetics Safety Assessment.

En Chine, la sécurité des ingrédients cosmétiques est réglementée par la NMPA (Administration Nationale des Produits Médicaux) conformément au CSAR (Règlement sur la Supervision et l'Administration des Produits Cosmétiques). Un ingrédient est considéré comme "nouveau" s'il ne figure pas dans l'IECIC 2021 (Inventaire des Ingrédients Cosmétiques Existants en Chine). Les ingrédients existants en Chine doivent être répertoriés dans l'IECIC 2021, et leurs données de sécurité doivent être rapportées à la NMPA via la plateforme d'information de sécurité des ingrédients cosmétiques.

On November 9, 2023, the European Union Scientific Committee on Consumer Safety (SCCS) published the preliminary opinion(SCCS/1658/23) on Hexyl Salicylate (CAS/EC No. 6259-76-3/228-408-6). The deadline for comments was set for 12 January 2024.

On November 6, 2023, the Scientific Committee on Consumer Safety (SCCS) of the European Union issued final opinion(SCCS/1657/23) on water-soluble zinc salts. The preliminary opinion on the safety of water-soluble zinc salts in cosmetics was released on July 4, 2023.

On November 7, 2023, the European Union Scientific Committee on Consumer Safety (SCCS) pulished the preliminary opinion(SCCS/1659/23) on Hydroxypropyl p-phenylenediamine and its dihydrochloride salt (CAS/EC No. 73793-79-0/827-723-1 and 1928659-47-5/-). The deadline for comments was set for 8 January 2024.