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Global Cosmetic Regulations Update — First Half of 2025
Publication date:2025-07-09

In the first half of 2025, cosmetic regulations worldwide have evolved steadily. From mature markets in Europe and North America to emerging Asian economies, countries have made updates to ensure consumer safety, protect the environment, and advance industry development. 

 

These changes affect product market access and consumer interests directly.

 

ZMUni Compliance Centre has summarized key regulatory updates from major markets, including the EU, US, Canada, South Korea and ASEAN.

 

Europe

 

On January 24, 2025, the European Commission updated the Borderline Manual to clarify that products in vials or ampoules with cosmetic functions—such as cleansing, fragrance, or appearance enhancement—and not intended for injection are classified as cosmetics.

 

On February 20, 2025, the French Parliament passed a law banning PFAS (per- and polyfluoroalkyl substances) in domestic markets, targeting cosmetics, textiles, and other products. Starting January 1, 2026, cosmetics containing PFAS will be prohibited from manufacture, sale, and import/export. The regulation does not list specific PFAS substances.

 

On April 1, 2025, the UK Office for Product Safety and Standards (OPSS) issued the 2025 Cosmetic Products (Restriction of Chemical Substances) Regulations, amending the UK Cosmetics Regulation (EC) 1223/2009 to add methyl salicylate to the list of restricted substances.

 

On May 8, 2025, the UK notified the WTO (G/TBT/N/GBR/102) of its plan to amend Annex VI of the UK Cosmetics Regulation (EC) 1223/2009 to restrict the use of Benzophenone-3 as a UV filter. The measure is set to take effect on January 21, 2026. Products placed on the market before that date may continue to be sold until July 21, 2026.

 

On March 13, 2025, the European Commission notified the WTO (G/TBT/N/EU/1116) of its plan to revise the Glossary of Common Ingredient Names for cosmetics and repeal the current Implementing Decision (EU) 2022/677. The revision aims to improve labeling consistency and ingredient identification accuracy. It is expected to be adopted in Q2 2025 and take effect 20 days after publication in the Official Journal of the EU.

 

On April 16, 2025, the EU released its 2024 Safety Gate report. Cosmetics made up 36% of alerts, with 97% containing banned fragrance BMHCA, known to harm reproduction and cause skin allergies.

 

On May 12, 2025, the European Commission adopted Regulation (EU) 2025/877, updating the EU Cosmetics Regulation to add newly classified CMR substances to Annex II (prohibited ingredients). Entry 311 of Annex III was also deleted, with its content moved to Annex II (Entry 1730). The regulation takes effect on September 1, 2025.

 

On May 21, 2025, the European Commission notified the WTO (G/TBT/N/EU/1140) of a proposed amendment to the EU Cosmetics Regulation (EC) No 1223/2009. The draft adds 15 CMR substances to Annex II and updates Annexes III, IV, and V. Based on Regulation (EU) 2024/2564, the amendment will take effect 20 days after publication and apply from May 1, 2026.

 

On May 21, 2025, the UK Scientific Advisory Group on Chemical Safety of Non-Food and Non-Medicinal Consumer Products (SAG-CS) published Opinion 18 on the use of 4-MBC as a UV filter in cosmetics. SAG-CS concluded that, based on current evidence, the safe use level of 4-MBC in cosmetics cannot be determined and its safety in sunscreens or other cosmetic products cannot be confirmed.

 

  • EU cosmetic ingredient bans in 2025

Ingredient

Deadline for placing on the market

Deadline for making available on the market

Styrene/Acrylates copolymer (nano) / Sodium Styrene/Acrylates copolymer (nano)

1 February 2025

1 November 2025

Copper (nano), Colloidal Copper (nano)

Colloidal silver (nano)

Gold (nano), Colloidal gold (nano) / Gold Thioethylamino Hyaluronic Acid (nano) / Acetyl heptapeptide-9 Colloidal gold (nano)

Platinum (nano), Colloidal Platinum (nano) / Acetyl tetrapeptide-17 Colloidal Platinum (nano)

4-Methylbenzylidene Camphor (4-MBC)

1 May 2025

1 May 2026

21 new CMR substances

The regulation takes effect on September 1, 2025.

 

  • EU cosmetic ingredient restrictions in 2025

Ingredient

Restriction

Deadline for placing on the market

Deadline for making available on the market

Homosalate

Face products, except propellant sprays, up to 7.34%.

1 January 2025

1 July 2025

Alpha-Arbutin

(a) Face cream, up to 2%;

(b) Body lotion, up to 0.5%.

1 February 2025

1 November 2025

Arbutin

Face cream, up to of 7 %.

Genistein

Up to of 0.007 %.

Daidzein

Up to 0.02 %.

Kojic Acid

Face and hand products, up to 1%.

Hydroxyapatite (nano)

(a) Toothpaste, up to 10 %;

(b) Mouthwash, up to 0.465%

(observe further restrictions in the column Other)

1 February 2025

1 November 2025

Retinol

(a) Body lotion,up to 0.05 % Retinol Equivalent (RE);

(b) other leave-on and rinse-off products, up to 0.3 % RE.

1 November 2025

1 May 2027

Retinyl Acetate

Retinyl Palmitate

 

  • EU SCCS Opinion released in 2025 H1

SCCS No.

Publication Date

Substance

Type

SCCS/1673/24

23 January 2025

HC Red No. 18

Final Opinion

SCCS/1672/24

1 April 2025

Benzophenone - 1

Final Opinion

SCCS/1674/25

2 May 2025

Butylparaben - Children's exposure

Final Opinion

SCCS/1675/25

2 May 2025

Salicylic Acid - Children's exposure

Final Opinion

SCCS/1676/25

2 May 2025

Methyl salicylate (methyl 2-hydroxybenzoate) - Children's exposure (Revision of SCCS/1654/23)

Final Opinion

SCCS/1671/24

30 June 2025

Ethylhexyl Methoxycinnamate (EHMC)

Final Opinion

SCCS/1678/25

30 June 2025

Diethylamino Hydroxybenzoyl Hexyl Benzoate (DHHB)

Final Opinion

SCCS/1679/25

30 June 2025

Benzophenone-2 (BP-2) and Benzophenone-5 (BP-5)

Final Opinion

SCCS/1680/25

6 June 2025

Methylamido-Dihydro-Noralfaprostal (MDN)

Preliminary Opinion open for comments

Isopropyl Cloprostenate (IPCP)

Dechloro Dihydroxy Difluoro Ethylcloprostenolamide (DDDE)

SCCS/1681/25

6 June 2025

Tea Tree Oil

Preliminary Opinion open for comments

 

Besides, on April 1, 2025, SCCS published consultation document SCCS/2022/Q/039 seeking scientific advice on the hair dye 'Basic blue 99 (C059)'. The proposal limits Basic Blue 99 to a maximum concentration of 1% in non-oxidative hair dye formulations. The public consultation period lasts 9 months.

 

 

North America

 

On February 11, 2025, the United States notified WTO (G/TBT/N/USA/2187) of a proposal to amend WAC 173-339 to restrict intentional use of formaldehyde and formaldehyde releasers in cosmetics. The proposal includes a specific list of restricted formaldehyde releasers. If adopted, the restrictions will take effect on January 1, 2027.

 

Health Canada updated the Cosmetic Ingredient Hotlist by adding one new prohibited ingredient (Thioglycolic acid esters), one new restricted ingredient (Retinal), revising the prohibition on mixed cresols and derivatives, and updating restrictions on peroxide compounds, benzoyl peroxide, and retinol esters.

 

On March 6, 2025, Health Canada launched its updated Cosmetic Notification System, featuring key improvements such as new fields for product use directions and warnings, language preference options for notifiers, expanded contact types with address verification, enhanced ingredient name requirements with INCI search, and options to submit detailed label documents. Manufacturers and importers must provide a Canadian address to comply.

 

On March 11, 2025, the U.S. Food and Drug Administration (FDA) published a statement regarding its testing of 95 acne products containing benzoyl peroxide to evaluate potential benzene contamination. The results revealed that over 90% of the samples either showed no detectable benzene or had only trace amounts. Only a few products were flagged for recall from retail stores.

 

On May 14, 2025, Health Canada issued a notice proposing updates to the Cosmetic Ingredient Hotlist—a list of substances that are prohibited or restricted in cosmetic products in Canada. The proposed amendments are adding 3 ingredients and revising 4 ingredients.

 

On May 20, 2025, the U.S. FDA convened an independent panel of international experts to assess the safety and necessity of talc in food, drug, and cosmetic products. The panel reached a unanimous decision in favor of banning talc, citing safety concerns across all product categories.

 

  • Multiple U.S. States enforce bans on PFAS in cosmetics

While the U.S. federal regulation of cosmetic ingredients remains limited, more states have introduced their own restrictions. In 2025, PFAS bans in cosmetics are taking effect across several states. See the table below for details.

State

Effective Date

Prohibited Substance

California

Jan 1, 2025

Twelve high-risk substances—including formaldehyde, mercury, PFAS and their salts

Maryland

Jan 1, 2025

Twelve high-risk substances—including formaldehyde, mercury, PFAS and their salts

Minnesota

Jan 1, 2025

Per- and polyfluoroalkyl substances (PFAS)

Colorado

Jan 1, 2025

Per- and polyfluoroalkyl substances (PFAS)

Washington

Jan 1, 2025

Nine high-risk substances — including per- and polyfluoroalkyl substances (PFAS), phthalates, and others

 

On June 3, 2025, the U.S. House Committee on Energy and Commerce received the SAFE Sunscreen Standards Act (H.R. 3686), led by Rep. John Joyce. The bill aims to amend the Federal Food, Drug, and Cosmetic Act to modernize and streamline the review process for OTC sunscreen active ingredients.

 

 

Asia

 

On January 2, 2025, South Korea's MFDS launched an AI-powered cosbot pilot project to offer customized information on domestic and international cosmetic regulations and banned ingredients, supporting Korean cosmetic exports and advancing the K-beauty industry throughout 2025.

 

On January 13, 2025, the MFDS announced a major increase in testing overseas online-sold cosmetics—from 110 items in 2024 to 1,080 in 2025—focusing on color and eye products for harmful substances. Non-compliant products may face sales bans and customs restrictions. The 2025 budget allocates 280 million KRW for these efforts, with recent tests showing multiple failures among color, eye, and nail cosmetics.

 

On January 31, 2025, Thailand published a notice in the Royal Gazette adding 56 substances—such as sodium perborate and nickel chloride—to its list of prohibited cosmetic ingredients (Entries No. 1613–1668). The changes took effect on February 1, 2025, aligning national regulations with recent updates to the ASEAN Cosmetic Directive (ACD). A 180-day grace period is granted for companies to reformulate products already produced, imported, or sold before the announcement.

 

On February 14, 2025, the MFDS published a Q&A clarifying labeling principles for cosmetic outer packaging based on recent Cosmetics Act amendments. It explains when required information can appear on outer packaging, highlighting that transparent packaging may display details without opening, but the guidance is for reference only and not legally binding.

 

On February 17, 2025, Indonesia's BPOM introduced new rules requiring 12 key labeling details, banning medical terms and healthcare images in ads, and enhancing oversight with monthly and surprise inspections. Non-compliance can lead to product bans, recalls, destruction, and public disclosure. Consumers are urged to report violations through official channels.

 

On March 26, 2025, South Korea's MFDS issued three public consultations (Announcements No. 111, 112, and 113) proposing to repeal regulations on natural and organic cosmetics certification.

 

On March 26, 2025, MFDS officially implemented regulations on lifting or modifying bans and on designating or changing cosmetic ingredient standards, offering clearer guidance for companies submitting related applications.

 

On March 18, 2025, the Philippines FDA issued Circular No. 2025-002, announcing updates to the ASEAN Cosmetic Directive following the 39th ASEAN Cosmetic Committee Meeting. Key changes include adding DEET to the banned substances list, amendments to restricted substances, inclusion of Acid Yellow 3 with conditions, updated criteria for CMR substances, and a review of ACD annexes.

 

On April 2, 2025, South Korea's National Assembly passed the Synthetic Biology Promotion Act, the first law globally dedicated to synthetic biology. The law will take effect in 2026 after cabinet approval, with supplementary legislation and guidelines to be developed during the one-year preparation period.

 

On April 28, 2025, the Indonesian Food and Drug Supervisory Agency (BPOM) released the 2025 legislative plan which includes finalized and draft amendments as well as new regulations. Regulations related to cosmetics covers areas such as cosmetic notification, ingredient requirements, labeling testing, production, and both online and offline distribution.

 

On May 8, 2025, JAKIM announced that electronic halal certificates (e-Certs) for the Malaysian Halal Certification Scheme (SPHM) have been effective since May 5, 2025.

 

On May 15, 2025, Vietnam's Ministry of Health released Draft Decree No. 2935/BYT-QLD, covering classification, notification, manufacturing, import/export, labeling, advertising, quality control, and recalls for cosmetics. The regulation will take effect on July 1, 2026, with a transition period allowing existing certificates until June 30, 2028, after which re-notification under the new rules will be required.

 

On May 16, 2025, Vietnam's Drug Administration (DAV) issued Official Dispatch No. 2965 urging stronger action against counterfeit, smuggled, and substandard cosmetics. On May 20, DAV followed with Notice No. 1372, focusing on enhanced post-market surveillance of sunscreens to combat non-compliance, false claims, and improper notifications, aiming to protect consumers and uphold industry trust.

 

On June 2, 2025, BPOM released a draft regulation to enhance safety and quality control of imported cosmetics by specifying mandatory test parameters for Certificates of Analysis (CoA) in the import certification process, signaling stronger regulatory oversight.

 

On June 19, 2025, South Korea's MFDS issued Notification No. 2025-258 proposing amendments to the Enforcement Rule of the Cosmetics Act to strengthen oversight of cosmetics bought directly from overseas, including risk disclosure, mandatory testing, and consumer usage surveys. Public consultation is open until July 30, 2025.

 

 

 

*Note: This article is compiled by ZMUni Compliance Centre, drawing from the latest updates from official regulatory authorities in various countries and regions. For any questions regarding interpretations or expressions, please consult the official real-time announcements.

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