US Court Limits California Prop 65 Warnings for Titanium Dioxide

An August 2025 federal court ruling in a case brought by the Personal Care Products Council (PCPC) has significantly changed how cosmetics and personal care companies approach California Proposition 65 compliance involving titanium dioxide. The U.S. District Court for the Eastern District of California issued a permanent injunction: –  preventing California authorities and private enforcers from pursuing new Prop 65 […]

USA – Dietary Supplement Regulatory Uniformity Act to proclaim FDA authority over Dietary Supplement’s regulations

  Dietary Supplement Regulatory Uniformity Act to proclaim FDA authority over Dietary Supplement’s regulations       If enacted, the Dietary Supplement Regulatory Uniformity Act proposed in February 2026 will amend the Federal Food, Drug, and Cosmetic Act (FDCA), and it will affirm the FDA’s authority over Dietary Supplements and their regulation.     The […]

U.S. FDA Withdraws Proposed Testing Rule for Talc-Containing Cosmetics

End of last year, the U.S. Food and Drug Administration (FDA) issued an unpublished notice titled “Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products; Withdrawal,” formally withdrawing its previously proposed rule on this topic. The withdrawal took effect upon the issuance of the notice. Under the now-withdrawn proposal, FDA had considered establishing specific […]

FDA Proposes Adding Bemotrizinol to the List of Permitted Sunscreen Active Ingredients

The U.S. Food and Drug Administration (FDA) has issued a proposed order that would add bemotrizinol to the list of permitted sunscreen active ingredients. According to the FDA: – bemotrizinol provides broad-spectrum UV protection and demonstrates low systemic absorption. – Bemotrizinol has a low irritation potential– if the proposed order is finalized, it would be […]

USA – FDA’s RFI on Future Gluten Labelling Regulations

    Back in January, the US Food and Drug Administration (FDA) issued a Request for Information (RFI) to gather input on potential gaps in the current gluten labelling framework.       Currently, products labelled “gluten-free” must contain less than 20 ppm of gluten. However, manufacturers are not required to disclose all gluten-containing grains […]

USA – Labels Amendments and Amazon’s New Certification Requirements

  DSHEA label disclaimer     On December 11th, the U.S. Food and Drug Administration (FDA) released a letter to the Dietary Supplement industry confirming that it is considering amending 21 CFR 101.93(d) in response to several requests to change the current labelling regulation.     As mandated by the Dietary Supplement Health and Education Act […]

USA – FDA Launches Dashboard for Cosmetic Product Adverse Events

On September 12, 2025, the U.S. Food and Drug Administration (FDA) announced the launch of the FDA Adverse Event Reporting System (FAERS) Public Dashboard for Cosmetic Products — a new tool designed to improve transparency and give the public real-time access to adverse event data related to cosmetics. This initiative is part of the FDA’s […]

USA – NMN exclusion | FDA’s Proposed Changes to GRAS

    NMN is (again) Legal in Dietary Supplements     At the end of last month, after nearly three years of discussions, the U.S. Food and Drug Administration (FDA) announced its position that nicotinamide mononucleotide (NMN) is not excluded from the legal definition of a dietary supplement.     Previously, the FDA had taken […]

Europe/US – New trade deal introduces 15% tariff on european imports

Recently, U.S. President Donald Trump announced a trade agreement with European Commission President Ursula von der Leyen, introducing a 15% import tariff on EU goods entering the U.S. market. This follows a similar agreement made by the UK in May, which imposed a 10% tariff on its exports to the U.S. While reaching an agreement […]

USA: Tariff-Exempt Dietary Ingredients | FDA Opinion on New Dietary Ingredients | FDA & the Potential Halt of GRAS Process | Restriction on the Sale of Dietary Supplements to Children and Adolescents

      Dietary Ingredients Exempt from Global and Reciprocal Tariffs Although some Global or Reciprocal Tariffs may be suspended for 90 days, certain Dietary Supplement ingredients have been declared exempt. According to Annex II of the executive order that implemented these tariffs, the following dietary ingredients are exempt: Vitamin A Vitamins B1, B2, B5, […]