Etiquetagem

A minimalist still life photography of various aromatherapy bottles on a white table.
Tailândia

Thailand Implements Emergency Facilitation Measures: 1-Day Fast-Track for Cosmetic Formula and Packaging Modifications

Amid ongoing geopolitical tensions in the Middle East causing significant cross-border logistics hurdles and disruptions in petro-chemical derivatives (such as plastic pellets and raw solvents), the Thai Food and Drug Administration (Thai FDA) officially implemented temporary regulatory flexibilities. Following a baseline framework announcement, the Thai FDA issued specific implementing guidance documents and fast-track application templates. These measures establish simplified paths, fast-track approvals, and exemptions from full re-notifications to ensure that cosmetic manufacturers and importers can swiftly adapt their formulations and packaging configurations to avoid supply chain disruptions. I. Raw Material and Formulation Facilitation Measures To accommodate rapid changes in international ingredient sourcing, the Thai FDA has established a multi-tiered track system based on the nature of the formulation change: 1. Modification of Raw Material Sources $\rightarrow$ No Re-Notification Required 2. Minor Formulation/Ingredient Modifications $\rightarrow$ 1-Day Fast-Track 3. Fragrance Realignment $\rightarrow$ Case-by-Case Review II. Packaging Modifications and Structural Flexibilities Recognizing acute

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Modern minimalist cosmetic setup with natural shadows creating an elegant feel.
Brasil

Brazil Issues New MERCOSUR “Net Content Labeling” Draft Regulations for Cosmetics: Major Changes for Gel Products

Have you ever noticed whether a cosmetic product package lists its net content in “grams” or “milliliters”? Behind that small print lies a strict set of technical regulations. Recently, Brazil’s National Institute of Metrology, Quality and Technology (Inmetro) published a major draft proposal aimed at comprehensively updating the quantitative labeling rules for cosmetics across the Southern Common Market (MERCOSUR/Mercosul). This update is crucial for export compliance and directly impacts consumer transparency. I. Regulatory Background: Overhauling a 22-Year-Old Rule On April 24, 2026, Inmetro published Public Consultation No. 8 in the Diário Oficial da União (Brazil’s Federal Official Gazette), introducing a new draft of the MERCOSUR Metrological Technical Regulation on the Quantitative Indication for Cosmetics (Draft Resolution No. 02/25). This draft is designated to replace the long-standing GMC Resolution No. 50/00, which has been in effect since 2000, bringing regional requirements in line with modern market developments and international standards under

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Three colorful ISDIN sun protection bottles against a blurred background, showcasing vibrant packaging.
Austrália

Regulatory Shifting Gears: TGA Releases Consultation on Overhauling Australian Sunscreen Oversight

On March 26, 2026, the Australian Therapeutic Goods Administration (TGA) published a comprehensive notice titled “Seeking to Improve the Regulation of Sunscreens in Australia.” This 8-week public consultation stems from Australia’s persistently high incidence of skin cancer and targets deep-seated loopholes in the current oversight framework. Stakeholders must submit their feedback by May 23, 2026. Additionally, a public webinar will be hosted on April 14, 2026, at 1:00 PM (AEST) featuring an expert panel Q&A session to dissect the critical proposals. I. Strategic Context and Drivers for Reform 1. Current Regulatory Landscape Australia categorizes sunscreens into two distinct streams based on their primary function: 2. Core Drivers for the 2026 Reform II. Scope of the Consultation III. Crucial Reform Modules and Proposed Options The TGA has laid out nine distinct reform modules, each weighing the status quo against more rigorous regulatory alternatives: Module 1: SPF Testing Methodologies Module 2: SPF

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White cosmetic containers and small vase on a pink background showcasing modern design and simplicity.
EUA

The Virginia State Humane and Toxin-Free Cosmetics Act: New Prohibitions on High-Risk Ingredients

The Virginia General Assembly introduced a significant legislative proposal designated as House Bill 122 (HB 122), titled the Virginia State Humane and Toxin-Free Cosmetics Act. This legislation amends existing trade laws to prohibit the manufacture, sale, and distribution of cosmetic products containing specific hazardous chemical substances within the Commonwealth. I. Core Legislative Provisions 1. Establishment of the “Toxin-Free Cosmetics” Article The bill introduces Article 2 (“Toxin-Free Cosmetics”) into Chapter 52 of Title 59.1 of the Code of Virginia, establishing a structured framework across the following statutory sections: 2. Schedule of Prohibited Chemical Substances Pursuant to § 59.1-574.2, no individual or corporate entity may manufacture, sell, deliver, offer for sale, or utilize in consumer transactions any cosmetic product containing the following intentionally added substances: No. Banned Substance Name CAS Registry Number 1 Dibutyl phthalate 84–74–2 2 Di(2-ethylhexyl) phthalate 117-81-7 3 Formaldehyde 50–00–0 4 Paraformaldehyde 30525-89-4 5 Methylene glycol 463-57-0 6 Quaternium-15

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Beautiful view of Wat Arun temple by the river in Bangkok during sunset.
Tailândia

Interpretation of Thailand’s Microneedle Cosmetic Regulations: Compliance Differences at a Glance

A Administração Tailandesa de Alimentos e Medicamentos (Thai FDA) publicou recentemente uma infografia oficial sobre os requisitos regulamentares para cosméticos à base de microagulhas. O principal objetivo é esclarecer que tipos de microagulhas são permitidos como cosméticos e quais são estritamente proibidos. Segue-se uma análise dos pontos essenciais da política: I. Limites regulamentares para os produtos com microagulhas 1. Patches de microagulhas que se dissolvem - permitidos como cosméticos 2. Microagulhas / microespículas que não se dissolvem - proibidas como cosméticos II. Acções de Conformidade Essenciais para as Empresas III. Sanções por Incumprimento (Regulamentos Locais Tailandeses) Assunto Medidas Sancionatórias Fabricante / Importador / Distribuidor Até 2 anos de prisão e/ou uma multa de 200.000 Baht Retalhista Até 6 meses de prisão e/ou uma multa de 50.000 Baht IV. Resumo de Conformidade Simplificado Tipo de Produto Estado de Conformidade Requisitos Principais Consequências da Violação Patch de Microagulha Dissolvente ✅ Permitido Comprimento da agulha $\le$ 100 $\mu$m; sem alegações médicas; registado como cosmético geral. As alegações ilegais são penalizadas

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