n this episode, we cover Indonesia’s 2026 Legislative Plan for cosmetic regulation, as announced by the National Agency of Drug and Food Control (BPOM). The plan outlines key areas of regulatory focus for the year, including improvements to the cosmetic notification system, updates to Good Manufacturing Practice (GMP) requirements, and refinements to importation control procedures. These initiatives aim to modernize Indonesia’s cosmetic regulatory framework, strengthen product quality oversight, and enhance compliance efficiency. We explain what the plan includes and why cosmetic manufacturers, brand owners, and import agents should pay attention to these upcoming changes.
For full details and expert insights, visit  https://cosmetic.chemlinked.com/news/cosmetic-news/indonesia-announces-2026-legislative-plan-covering-cosmetic-notification-gmp-and-importation?utm_source=podcast

 In this episode, we cover the European Union Scientific Committee on Consumer Safety’s (SCCS) recent final opinions identifying safety risks associated with several cosmetic ingredients. Released on February 10, 2026, the SCCS determined that certain prostaglandin analogues used in eyelash and eyebrow growth products, Basic Blue 99 and Basic Brown 16 in non-oxidative hair dyes, and the preservatives Thiomersal and Phenylmercuric salts cannot be considered safe for use in their relevant cosmetic product categories. These conclusions reaffirm concerns from preliminary assessments and may have regulatory implications for ingredient usage and formulation compliance in EU cosmetic markets.
For full details and continuous regulatory insights, please click at EU SCCS Identifies Safety Risks in Prostaglandin Analogues, Basic Blue 99, Basic Brown 16, Thiomersal, and Phenylmercuric Salts  

 In this episode, we cover proposed amendments to the South Korea Cosmetics Act aimed at regulating environmental claims and standardizing cosmetic product labeling. South Korea’s Ministry of Food and Drug Safety has released a draft that would require clearer criteria and evidence for environmental or sustainability claims on cosmetics, and ensure consistent labeling practices across the market. We explain what the draft entails, why it matters for cosmetic manufacturers and marketers. For full details and regulatory updates, please click South Korea Proposes Amending Cosmetics Act to Regulate Environmental Claims and Standardize Labeling 

 The UK has amended its Cosmetics Regulation, adding 13 CMR substances to the prohibited list and introducing new concentration limits for Hexyl Salicylate, including specific limits for fragrance, rinse-off, leave-on, oral care, and nail products.

In this episode, ChemLinked breaks down:

• The effective dates and sell-through periods
• The list of newly prohibited CMR substances
• Detailed restriction requirements for Hexyl Salicylate
• What these changes mean for compliance planning

Stay informed on global cosmetic regulatory developments.

For full regulatory tables and in-depth analysis, please click UK Amends Cosmetics Regulation with New Ingredient Prohibitions and Restrictions

 In this episode, we discuss the draft regulation notified by Indonesia to the World Trade Organization (WTO) on February 12, 2026, concerning non-halal labeling requirements for consumer products including cosmetics. Under WTO notification G/TBT/N/IDN/184, the draft — open for public comments until March 14, 2026 — specifies when a product must carry a standardized “NON HALAL” mark on its label. Criteria for determining non-halal status are based on ingredient origin and production methods. This update aims to provide clearer guidance for how non-halal products are presented to consumers in the Indonesian market.
For full details and ongoing regulatory insights, please click at Indonesia Details Non-Halal Labeling Rules for Cosmetics

 In this episode, we cover China’s National Institutes for Food and Drug Control (NIFDC) public consultation on six draft cosmetic testing methods released on February 3, 2026. These methods — which include procedures for acrylates (HPLC), chromium speciation (LC-ICP-MS), aristolochic acids, formaldehyde-releasing preservatives, diethanolamine, and silica nano-particle detection — are intended to standardize analytical practices in cosmetics laboratories and regulatory testing. The consultation is open until March 5, 2026, and stakeholders can submit feedback through China’s cosmetic standards management system. We explain the key methods being proposed and why accurate testing standards are essential for compliance.
For full consultation details and expert analysis, please click at China NIFDC Consults on Six Draft Cosmetic Testing Methods 

 In this January 2026 Monthly Recap, ChemLinked reviews key cosmetic regulatory developments across the Chinese Mainland, South Korea, Malaysia, Indonesia, India, New Zealand, the European Union, the United States, and Brazil. Major highlights include China’s IECIC update and new testing methods, South Korea’s proposed AI advertising restrictions, Malaysia’s ingredient annex amendments, Indonesia’s pharmaceutical-grade ingredient proposal, New Zealand’s updated Cosmetic Products Group Standard, the EU’s ban on 15 CMR substances effective May 2026, U.S. PFAS legislation and FDA MoCRA guidance, and Brazil’s consultation on cosmetic fractionation rules.

This episode provides a structured overview of global compliance trends shaping the cosmetic industry in early 2026.

For detailed regulatory analysis and continuous updates, visit  https://cosmetic.chemlinked.com/news/cosmetic-news/monthly-recap-global-cosmetic-regulatory-updates-january-2026?utm_source=podcast

 In this episode, we cover Indonesia’s draft regulation that specifies pharmaceutical-grade ingredient requirements for certain natural medicines, health supplements, quasi-drugs, and dental and oral care cosmetic products. Released by the Indonesian Food and Drug Supervisory Agency (BPOM) on January 27, 2026, the draft outlines a list of 14 ingredients, such as glycerin, polyethylene glycol derivatives, propylene glycol, sorbitol, and related compounds, that must comply with pharmaceutical-grade standards when used in designated product categories. The regulation builds on BPOM’s earlier risk assessment framework and aims to enhance ingredient quality and safety in higher-risk cosmetic applications. Stakeholders are invited to submit comments by February 10, 2026.
For full details and expert insights, please click at Indonesia Details Pharmaceutical-Grade Ingredient Requirements for Dental and Oral Care Products 

 In this episode, we cover a recent statement from Australia’s Therapeutic Goods Administration (TGA) regarding sunscreen labeling practices. The TGA clarifies expectations for how sunscreen products should be labeled and presented to consumers in the Australian market, including accurate SPF claims, broad-spectrum protection statements, and the avoidance of misleading or unapproved performance assertions. We discuss why this statement matters for manufacturers and brand owners and how it supports consumer understanding and regulatory compliance.
For full details and continuous regulatory updates, please click Australia TGA Issues Statement on Sunscreen Labelling Practices 

 In this episode, we cover Malaysia’s latest amendment to its cosmetic ingredient requirements. The National Pharmaceutical Regulatory Agency (NPRA) has updated the Guidelines for Control of Cosmetic Products, introducing four new ingredient additions and one deletion to the relevant annexes. These changes may involve updated use conditions, concentration limits, and compliance requirements for cosmetic manufacturers and brand owners marketing products in Malaysia. As Malaysia operates within the ASEAN Cosmetic Directive framework, this amendment also reflects ongoing regional regulatory alignment.

For full details and expert regulatory insights, please click Malaysia Amends Cosmetic Ingredient Use Requirements: 4 Additions and 1 Deletion