by Guido Rainis | Mar 1, 2024 | USA
Cosmetic products marketed in the USA, whether domestically manufactured or imported, must comply with the requirements of the Federal Food, Drug, and Cosmetic Act (FD&C Act) and Fair Packaging and Labeling Act (FP&L Act). The label elements required under the...
by Guido Rainis | Nov 8, 2023 | USA
As previously reported, the submission of information about existing facilities who are marketing cosmetic products in the US, and listing of their cosmetic products according to MoCRA will be required from 29th December 2023. The FDA is about to set up an electronic...
by Guido Rainis | Nov 3, 2023 | USA
As previously reported, the submission of information about existing facilities who are marketing cosmetic produscts in the US, and listing of their cosmetic products according to MoCRA will be required from 29th December 2023. The FDA is about to set up an electronic...
by Guido Rainis | Aug 10, 2023 | USA
On 7th August 2023, the US Food and Drug Administration (FDA) issued the draft guidance on cosmetic product facility registrations and products[1], following the Modernization of Cosmetics Regulation Act (MoCRA) passed by the Congress and signed by the President as...
by Guido Rainis | Aug 9, 2023 | EU
Regulation (EU) 2023/1545 was published on 26th July 2023[1], regarding labelling of fragrance allergens in cosmetic products. It introduces 56 new fragrance substances to Annex III, plus updates to some already existing entries. The new Regulation follows the SCCS...