China Launches Cosmetic E-Label Pilot Program
China’s cosmetic regulatory framework is entering a new digital phase with the official launch of the Cosmetic E-Label Pilot Program, effective 1 February 2026. An E-Label is a compliant, scannable QR code that functions as a digital extension of the physical cosmetic label. It is a mandatory component of the product label, not an optional alternative. Essential information—such […]
Indonesia Proposes Pharmaceutical-Grade Requirements for Certain Cosmetic Ingredients
On 27 January 2026, Indonesia’s Food and Drug Supervisory Agency (BPOM) released a draft regulation introducing a List of Pharmaceutical Ingredients Used in Natural Medicines, Health Supplements, Quasi-drugs, and Certain Cosmetic Products. The draft regulation identifies specific ingredients that must meet pharmaceutical-grade standards when used in designated: Natural medicines, Health supplements, Quasi-drugs and Certain cosmetic products. The proposal follows […]
Malaysia Tightens Regulation of Aesthetic and Cosmetic Medical Devices
On 9 January 2026, Malaysia’s Medical Device Authority (MDA) issued the Medical Device (Prescribed Medical Device) Order 2026, strengthening oversight of medical devices used for aesthetic and cosmetic purposes. The regulation will take effect on 1 June 2026. The order covers devices such as laser treatment systems, high-intensity focused ultrasound (HIFU) devices, liposuction equipment, and other related […]
New Zealand Updates Cosmetic Import and Manufacturing Rules
On 21 January 2026, New Zealand’s Environmental Protection Authority (EPA) confirmed that updated rules governing the import and manufacture of cosmetic products took effect on 1 January 2026 under the revised Cosmetic Products Group Standard 2020. The changes apply to a wide range of cosmetics, including soaps, shampoos, toothpaste, deodorants, perfumes, make-up, sunscreens, insect repellents and self-tanning […]
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 […]
Brazil: Anvisa Launches Public Consultations on Repackaging and Packaging Reuse for Cosmetics
On 20 January 2026, the Brazilian Health Regulatory Agency (Anvisa) launched two public consultations (No. 1380 and No. 1381) addressing the repackaging and reuse of packaging for personal care products, cosmetics, and perfumes. The consultations set out proposed technical requirements and Good Manufacturing Practices (GMP) applicable to these activities and define the product categories eligible for repackaging and packaging reuse. […]
France Introduces PFAS Ban
End of last year, France published Decree No. 2025-1376 on the prevention of risks resulting from exposure to perfluoroalkyl and polyfluoroalkyl substances (PFAS). The decree implements Articles L. 524-1 and L. 524-2 of the Environmental Code, as amended by Law No. 2025-188 of 27 February 2025, which aims to protect the population from health and environmental […]
Indonesia: BPOM Issues New Requirements for Certificates of Analysis for Import Licences
On December last year, Indonesia’s National Agency of Drug and Food Control (BPOM) issued Decree No. 627/2025, updating the requirements for the Certificates of Analysis (CoA) submitted as part of an application for an import licence (SKI). Under the SKI framework, a CoA is mandatory and must be issued either by the product manufacturer or by an accredited […]
Omnibus Act VIII – Further upcoming restrictions
The European Union is introducing significant changes to cosmetic ingredient regulations under Omnibus Act VIII, which will take effect on May 1, 2026. The above Act expands the list of substances classified as Carcinogenic, Mutagenic, or Toxic for Reproduction (CMRs) that are either banned or subject to strict restrictions in cosmetic products. All non-compliant cosmetic products must […]
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 […]
