Compliance
Cosmetic regulations by market, with the latest amendments
42 markets, isa ang bawat card: ang awtoridad, notification vs registration, sino ang dapat maging local responsible person, ano ang kailangan ng safety file, ang mga pangunahing labeling rules, at ang pinakabagong pagbabago. Kapag ang banned/restricted list ng isang market ay nasa aming inventories, direkta itong nakakonekta.
Bawat entry ay may pinagmulang opisyal o industry source; ang opisyal na teksto ng bawat market ang nangingibabaw at ito ay factory-side digest, hindi legal advice. Data updated 2026-09-10.
Latest changes, 2025–2026
Pinakabago muna; lamang ang mga pagbabago na nasa lakas o may naipublikadong petsa. C · Opisyal na pinagmulan
Unyon Europeo · Ang pagpapalawak ng EU sa pagpapalamang ng alerhena ng pabango ay naging mandatory para sa mga bagong produkto
Regulation (EU) 2023/1545 adds 56 allergens to Annex III; products placed on market from 31 July 2026 must name them above 0.001% (leave-on) / 0.01% (rinse-off), with existing products to comply by 31 July 2028 — Switzerland applies the same annex and Canada mirrors the list.
SourcesMainland China · Ang China NMPA Announcement No. 70 (2026) ay pinapadali ang rehistrasyon at pagpaplano
Eight measures: a first-launch-in-China commitment replaces home-market sale proof, animal-test exemptions widen, ingredient safety data are archived instead of submitted, similar formulas may share test reports, cross-border production transfers and domestic-responsible-person changes are simplified, and more efficacy-test methods are accepted.
SourcesUnited Kingdom (Great Britain) · Ang UK SI 2026/23 at SI 2026/109 ay nagtatakda ng mga bansa at petsa na tiyak sa GB
Great Britain bans 4-MBC and lowers the formaldehyde-releaser warning threshold to 0.001% from 15 July 2026, bans CMRs incl. TPO from 15 August 2026 (sell-through to 14 February 2027), restricts hexyl salicylate from 15 August 2026 and bans 17 more CMRs incl. nano silver from 23 March 2027, while still not adopting the EU 2023/1545 allergen expansion.
SourcesTaiwan · Ang Taiwan ay ginawang mandatory ang PIF at GMP para sa lahat ng pangkaraniwang kosmetiko
The final phase of the Cosmetic Hygiene and Safety Act roll-out requires every general cosmetic (except exempt handmade soap) to hold a Product Information File with a safety assessment and to be manufactured under 化粧品優良製造準則, on top of the existing product notification.
SourcesASEAN (ASEAN Cosmetic Directive) · Ang ASEAN ay naglabas ng na-revise na ACD Annexes II, III, IV at VI
Pagkatapos ng 43rd ACC meeting, ang bifonazole, clotrimazole, thiabendazole at tioconazole ay ipinagbawal, ang kojic acid ay limitado sa 1%/0.2%, ang BHT at verbena absolute ay pinaghihigpitan, at ang chlorophene/2-chloroacetamide ay tinanggal bilang preservative; ang Malaysia ay ipinasa ang mga pagbabago sa pamamagitan ng NPRA Circular 2/2026 noong 2026-07-06 at ang Pilipinas ay kinumpirma na ang mga pagbabago ng 40th–42nd ACC sa pamamagitan ng FDA Circular 2026-0001 noong 2026-04-22.
SourcesAustralia · Ang Australia ay nangangailangan ng AICIS assessment certificate para sa retinal sa mga produkto para sa consumer
Following evaluation EVA00186 (presumed developmental toxicant, Repr. 1B), retinal/retinaldehyde with any consumer end use can no longer be exempted or reported, so an assessment certificate is needed before import or manufacture of retinal serums, creams and moisturisers.
SourcesBangladesh · Ang Bangladesh ay naglabas ng draft Cosmetics (Licence and Registration) Rules 2026
Inilabas ng Health Services Division para sa komento ang draft na mga patakaran na gagawing operasyonal ang paglilisenso at pagrehiistro ng mga kosmetiko sa ilalim ng Drugs and Cosmetics Act 2023 (DGDA), na hanggang ngayon ay tumatakbo nang walang detalyadong patakaran.
SourcesBrazil · Ang Brazil ay naglabas ng RDC 1.029/2026 at 1.030/2026 na mga listahan ng sangkap pagkatapos ng 2025 bans
Ang bagong restricted list ng ANVISA na harmonisado sa Mercosur (part 1, 24-month adaptation) at prohibited list (12-month adaptation) ay sumusunod sa TPO at DMPT ban ng RDC 995/2025 na naka-effect noong 2025-11-03 at sa animal-testing ban ng Law 15.183/2025 mula 2025-07-31; ang consultation 1.399/2026 para sa ikalawang tranche ng restricted list ay tumagal hanggang 8 September 2026.
SourcesUkraine · Ang Ukraine ay kinumpirma ang Resolution No. 737 na nagbabago sa Technical Regulation ng kosmetiko
Re-issues Annexes 2–6 to EU 1223/2009 levels, keeps 2026-08-03 as the date from which all newly placed cosmetics must be notified and fully compliant, allows legacy/non-notified stock to be sold until 2030-08-03, and enters into force six months after publication (2026-12-13).
SourcesUnyon Europeo · Regulation (EU) 2026/909 ('Omnibus Act 2') ay pumapasok sa lakas
Published 2026-04-28, it restricts fragrance allergens (benzyl salicylate, citral/geranial/neral, acetylated vetiver oil), aluminium compounds, zinc salts and several hair dyes and bans triphenyl phosphate, with a placing-on-market deadline of 2027-01-01 and sell-through to 2028-07-01 (citral 2028-08-01).
SourcesArgentina · Argentina ay tumanggap ng Mercosur GMC 27/25, 06/25 at 07/25 lists at nagderegulate ng imports
Disp. 2820/2026 bans TPO and N,N-dimethyl-p-toluidine with 60 days to adapt; Disp. 2599/2026 and 2601/2026 (BO 2026-05-21) replace the 2011/2014 restricted and prohibited lists; earlier Disp. 4033/2025 removed ANMAT prior intervention on cosmetic imports from 2025-07-10 and Disp. 7939/2025 allowed establishment enabling by sworn declaration.
SourcesUnyon Europeo · EU Omnibus VIII (Regulation (EU) 2026/78) ay aplikado
Published 2026-01-13, it bans nano and massive silver, restricts silver powder, hexyl salicylate and o-phenylphenol, and required withdrawal of non-compliant products by 1 May 2026 without a stock-clearance period.
SourcesCanada · Canada ay nagpapatupad ng fragrance-allergen disclosure sa cosmetic labels
Under SOR/2024-63, 24 fragrance allergens must appear in the ingredient list above 0.001% leave-on / 0.01% rinse-off from 12 April 2026, expanding to 81 allergens for new products from 1 August 2026 and all products from 1 August 2028, with compliance promotion until 11 April 2027.
SourcesTimog Korea · Korea ay nagpapatupad ng mandatory cosmetic safety assessment system (Act No. 21302)
Ang mga responsible sellers ay dapat maghanda at magtago ng safety assessment na sinuri ng qualified assessor bago ang marketing; ang MFDS ay naglabas ng preparation guidelines noong 2026-06-10 at draft Decree/Rule amendments noong 2026-07-08, na may phased application mula 2028 at full enforcement tungkol sa 2031.
SourcesIsrael · Israel ay nagmungkahi ng 'U.S. track' at retailer duties para sa cosmetics
Ang isang legislative memorandum ng Ministry of Health ay papayagan ang importasyon ng mga FDA-compliant na kosmetiko kasabay ng EU track, maglalagay ng verification duties sa mga retailer sa pamamagitan ng MoH cosmetics database, ilalagay ang solid soap sa sakop, at gagawa ng standing advisory committee; ito ay nananatiling isang proposal.
SourcesUnited States · FDA ay bumaba ng talc-asbestos testing rule habang ang ibang MoCRA rules ay nananatiling pending
FDA withdrew the December-2024 proposed talc testing rule, issued its PFAS-in-cosmetics report (2025-12-29) and draft mandatory-recall guidance (2025-12-18); GMP, fragrance-allergen and formaldehyde hair-smoothing rules missed statutory deadlines with NPRMs now targeted for November 2026, and biennial facility-registration renewals began two years after each initial registration.
SourcesIndonesia · Indonesia ay naglabas ng PerBPOM 25/2025 tungkol sa cosmetic ingredients bago ang halal deadline
Issued in October 2025 (day inferred from its one-year transition ending 2026-10-03), PerBPOM 25/2025 replaced the 2019/2022 ingredient rules with tighter ACD-aligned limits; two weeks after that deadline, on 2026-10-17, BPJPH halal certification becomes mandatory for all cosmetics under PP 42/2024.
SourcesKazakhstan (EAEU member) · EEC Council Decision No. 74/2025 ay nagbabago sa TR CU 009/2011 ingredient annexes
Published 2025-10-28 and applicable across the EAEU (incl. Kazakhstan) from 2026-10-28, it adds 14 prohibited substances, three restricted substances, a new UV filter (incl. nano form) and bans fluorides in liquid oral products for children under 6, with a 0.001% formaldehyde labelling threshold from 2027-01-01; EEC Board Decision No. 31 (2026-03-10) set transition periods.
SourcesSaudi Arabia · SFDA ay nagbawal ng 21 pang cosmetic ingredients
After a 2025-08-14 circular adding three restricted substances, SFDA added 21 substances (e.g. dibutyltin maleate, dibutyltin oxide, 4-nitrosomorpholine, 4-methylimidazole) to its prohibited list; import/manufacture of non-compliant products is banned from 2026-01-01 with sell-through allowed until 2028-01-01.
SourcesUnyon Europeo · EU Omnibus VII (Regulation (EU) 2025/877) ay nagbawal ng TPO at ibang CMRs
TPO (UV nail-gel photoinitiator) and other newly classified CMR substances were added to Annex II with no sell-through: products may neither be placed nor made available on the EU market from 1 September 2025.
SourcesVietnam · Vietnam Circular 34/2025/TT-BYT ay pumapasok sa lakas; ang draft Cosmetics Decree ay nasa consultation
Ang Circular 34/2025 (inalabas 2025-07-03) ay nagdagdag ng online notification sa pamamagitan ng National Public Service Portal, habang ang draft Decree ng MoH tungkol sa Cosmetic Management (WTO G/TBT/N/VNM/349, na redrafted 2026-02 at 2026-05) ay magpapalit sa Circular 06/2011 na may mandatory CGMP-ASEAN, PIF at mas mahigpit na claims rules.
SourcesColombia / Andean Community (Bolivia, Colombia, Ecuador, Peru) · Andean Decision 944, mandatory labelling regulation at ang animal-testing rule ng Colombia
Decision 944 removes the blanket Spanish-translation requirement for NSO technical files; the Andean Labelling Technical Regulation (Res. 2310) became mandatory on 2025-12-17 for Colombia, Peru, Ecuador and Bolivia; Colombia's Res. 0814/2026 (May 2026) requires a first-party no-animal-testing declaration with new and renewed NSOs.
SourcesMorocco · Ang AMMPS ng Morocco ay nagkondisyon sa cosmetic applications sa updated establishment declarations
Ang mga application na isinumite simula 2025-06-11 ay pinroseso lamang pagkatapos ang cosmetics/body-hygiene establishment declaration ng operator ay na-update, bahagi ng DMP-to-AMMPS transition na layuning mataguyod ang bawat produkto sa isang responsible operator.
SourcesJapan · Japan ay nagpapatupad ng PMD Act amendment (Act No. 37 of 2025)
Phased in from 2025-11-20 and 2026-05-01, the amendment strengthens MAH quality/safety governance and supply obligations; the cosmetics-specific 2025 change was MHLW's 2025-03-10 notice rewriting the 特記表示 highlighted-ingredient rules to require the ingredient's purpose on packs and ads.
SourcesSri Lanka · Sri Lanka NMRA ay nagrevisyon ng document requirements para sa bagong cosmetic registrations
Ang bagong 11-document checklist para sa mga importer (heavy-metal CoA, steroid-free declaration, ISO 22716/GMP certificate, Safety Assessment Report, embassy-attested FSC) ay gagamit mula 2025-06-01.
SourcesMainland China · China ay huminto sa pagtanggap ng simplified safety assessment reports
The one-year transition under NMPA Announcement 2024 No. 50 ended, so every new registration or filing now needs a full-version safety assessment per the 2021 Technical Guidelines, with eligible general cosmetics submitting the basic conclusion and keeping the full report on file.
SourcesTimog Korea · Korea ay nagbabago sa cosmetic packaging labelling rules
Ang MFDS ay nag-amend sa Cosmetics Act Enforcement Rule (Annex 4) na may immediate effect, na nagrevisyon kung paano dapat lumabas ang manufacturing number, expiry date, period-after-opening at precautions sa lahat ng cosmetics na gawa o imported pagkatapos ng petsang iyon.
SourcesIsrael · Ang 'What is good for Europe' cosmetics reform ng Israel ay pumapasok sa lakas
Ang Amendment No. 37 (2024) sa Pharmacists Ordinance ay pinalitan ang cosmetic product licence (naitigil noong 2024-12-31) ng notification ng mga EU/UK/Swiss-compliant na kosmetiko ng isang rehistradong Israeli responsible representative, habang ang mga sensitive categories ay nananatili sa ilalim ng approval.
Sources
Middle East 5
GCC Standardization Organization (GSO) issues the Gulf Technical Regulation; national regulators (SFDA, MoIAT/municipalities, etc.) enforce it
GCC (Gulf Cooperation Council bloc: Saudi Arabia, UAE, Kuwait, Qatar, Bahrain, Oman)
GSO 1943:2024 (Edition 4, approved 2024-05-01); companions GSO 2528:2024 (claims), GSO 2636:2021 (PIF), GSO 2020:2010 (GMP) · GSO 1943:2024 Cosmetic Products – Safety Requirements of Cosmetics and Personal Care Products (Gulf Technical Regulation)
- In force
- 2009-10-17
- Pinakamabagong pagbabago
- GSO 1943:2024 (Edition 4) and GSO 2528:2024 on cosmetic claims approved, replacing GSO 1943:2021/2022.Sources
- Market entry
- No bloc-level system: each member state runs its own pre-market notification/conformity scheme against GSO 1943 (SFDA GHAD/eCosma in KSA, MoIAT ECAS plus Dubai Montaji in UAE, etc.).
- Responsible person
- GSO 1943 requires the manufacturer or responsible person's name/address on the label, and in practice every member state requires a locally licensed importer/agent to notify products.
- Safety file
- Product Information File per GSO 2636:2021 with safety assessment, formula, test data and GMP (GSO 2020 / ISO 22716) evidence, available to authorities on request.
- Labeling
- Arabic mandatory (Arabic-only or bilingual Arabic/English) with INCI ingredients, batch, expiry/PAO, country of origin and manufacturer/RP; products must be free of pork derivatives and must not carry imagery contrary to Islamic/GCC values; halal certification voluntary.
- Animal testing
- No GCC-wide ban on animal testing of cosmetics identified.
- Ingredient lists
- GSO 1943 annexes of prohibited substances, restricted substances, permitted colorants, preservatives and UV filters, aligned to EU Regulation (EC) No 1223/2009.
- Mga Tala
- GSO 1943 is adopted nationally (SFDA.CO/GSO 1943, UAE.S GSO 1943) and enforced by national authorities; consultancy claims of a 'unified GCC regulation 2026' cite no official GSO document, so no 2025-2026 bloc-level change is verified.
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Saudi Food and Drug Authority (SFDA)
Saudi Arabia
Royal Decree No. M/49 dated 18/6/1436H (2015-04-07); Implementing Regulation of the Cosmetic Products Law; SFDA.CO/GSO 1943:2024; SFDA.CO/GSO 2528:2024 · Cosmetic Products Law (Royal Decree No. M/49 of 18/6/1436H) and its Implementing Regulation, with technical requirements SFDA.CO/GSO 1943
- In force
- 2015-10-04
- Pinakamabagong pagbabago
- SFDA added 21 substances to its prohibited list (after a 2025-08-14 circular adding three restricted substances); import/manufacture of non-compliant products is banned from 2026-01-01 with sell-through allowed until 2028-01-01.Sources
- Market entry
- Mandatory pre-market product notification (listing) in the SFDA GHAD unified e-platform (eCosma module; GHAD replaced eCosma on 2023-03-30), decided within 15 days and valid 5 years, plus a shipment Certificate of Conformity via FASEH before customs clearance.
- Responsible person
- Only an SFDA-licensed Saudi establishment (importer/distributor or local manufacturer) can notify products, so foreign brands must appoint such a local agent.
- Safety file
- Product Information File per GSO 2636 with safety assessment, formula, test reports and GMP (GSO 2020 / ISO 22716) evidence held for SFDA inspection; local factories need an SFDA technical licence.
- Labeling
- Arabic labeling mandatory (bilingual Arabic/English accepted) with INCI list, function, batch, expiry or PAO, responsible party, net content, warnings and country of origin; must be free of pork derivatives; halal certification not legally mandatory.
- Animal testing
- No statutory ban on animal testing of cosmetics identified.
- Ingredient lists
- SFDA lists of prohibited and restricted substances and permitted colorants, preservatives and UV filters (SFDA.CO/GSO 1943 annexes aligned to EU 1223/2009), amended by SFDA circulars of Feb, Aug and Sep 2025.
- Mga Tala
- SFDA's own site blocked fetching, so the 2025 circular dates rely on SGS/Cotecna summaries; Cotecna's Feb-2025 item describes an earlier restricted-substances circular with separate deadlines of 2026-12-01 (production/import) and 2028-12-01 (market).
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Ministry of Industry and Advanced Technology (MoIAT, successor of ESMA) for ECAS conformity; Dubai Municipality (Montaji) and other emirate municipalities for product registration
United Arab Emirates
Cabinet Decision No. 18 of 2014; UAE.S GSO 1943:2024; GSO 2528:2024; Cabinet Decision No. 5 of 2014 (fragrances) · Cabinet Decision No. 18 of 2014 on the UAE Regulation for the Control of Cosmetics and Personal Care Products, applying UAE.S GSO 1943
- In force
- 2014-04-29
- Pinakamabagong pagbabago
- MoIAT updated its Technical Guidelines for Cosmetics and Personal Care Products and adopted GSO 1943:2024 / GSO 2528:2024 (effective 2024-05-01); no new federal cosmetics decision found for 2025-2026.Sources
- Market entry
- Two-layer pre-market system: MoIAT ECAS Certificate of Conformity (valid 1 year) against GSO 1943 for import/customs, plus product registration in Dubai Municipality's Montaji system (valid 5 years) before retail sale.
- Responsible person
- Only a UAE-incorporated entity (local manufacturer, importer or distributor) may hold ECAS certificates and Montaji registrations, so foreign brands need a local agent.
- Safety file
- Dossier with Free Sale Certificate, full ingredient report, GMP evidence and accredited lab test reports (microbiology, heavy metals), with a PIF per GSO 2636 held by the local registrant.
- Labeling
- Arabic labeling mandatory (bilingual Arabic/English accepted) per Cabinet Decision 18/2014 and GSO 1943 with INCI, batch, expiry/PAO, warnings and allergen declaration; pork-free and no imagery contrary to Islamic values; halal certification voluntary but required if halal is claimed.
- Animal testing
- No formal ban on animal testing of cosmetics in the UAE.
- Ingredient lists
- UAE.S GSO 1943 annexes (prohibited, restricted, colorants, preservatives, UV filters) aligned to EU 1223/2009.
- Mga Tala
- Consultancy reports say the Emirates Drug Establishment (Federal Decree-Law 28/2023) took over medicated-product registration from MOHAP at end-2025 while ordinary cosmetics stayed with Montaji; not verified on an official page. Montaji covers Dubai only; other emirates use their own municipal systems.
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Ministry of Health – Pharmaceutical Division (Cosmetics Department)
Israel
Pharmacists Ordinance (Amendment No. 37), 2024; Pharmacists' Regulations (Cosmetics) 5783-2022 (WTO G/TBT/N/ISR/1279) · Pharmacists Ordinance [New Version] 1981 as amended by Amendment No. 37 (2024) ('What is good for Europe is good for Israel' cosmetics reform), with the Pharmacists' Regulations (Cosmetics)
- In force
- 2025-01-01
- Pinakamabagong pagbabago
- MoH legislative memorandum proposes a parallel 'U.S. track' for FDA-compliant cosmetics, retailer verification duties against the MoH cosmetics database, and adding solid soap to the cosmetic definition (proposal, not yet law).Sources
- Market entry
- Since 2025-01-01 the old Cosmetic Product Licence (discontinued 2024-12-31) is replaced by online notification to the MoH (Notification Track) by a registered dealer/responsible representative; EU-, UK- or Swiss-compliant products qualify, while 'sensitive' cosmetics (children under 12, sunscreens, nano, hair straighteners, etc.) stay under stricter approval.
- Responsible person
- An Israel-resident Responsible Person/representative registered in the MoH database must be appointed and is legally liable for the PIF and product safety.
- Safety file
- EU-style Product Information File with Cosmetic Product Safety Report by a qualified assessor, GMP (ISO 22716) and test data, kept 10 years.
- Labeling
- Hebrew labeling mandatory (English/Arabic optional) with INCI, batch, expiry/PAO, responsible person details and warnings, traceable to the MoH notification/database entry.
- Animal testing
- Banned: testing cosmetics on animals in Israel since 2007 and import/marketing of animal-tested cosmetics since 2013-01-01.
- Ingredient lists
- Annexes aligned to EU Regulation 1223/2009 (prohibited, restricted, colorants, preservatives, UV filters).
- Mga Tala
- gov.il pages could not be fetched; the 2026 transition deadline for legacy licences and the Hebrew/English/Arabic label statement come from consultancy pages.
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Egyptian Drug Authority (EDA) – General Administration for Cosmetic Products Registration
Egypt
Law No. 151/2019; EDA Decree No. 122/2022 (effective 2022-02-27); Regulatory Guide for Cosmetics Notification (2023) · Law No. 151 of 2019 establishing the Egyptian Drug Authority, with EDA Chairman Decree No. 122 of 2022 on the listing (notification) and circulation of cosmetic products
- In force
- 2022-02-27
- Pinakamabagong pagbabago
- EDA issued the Regulatory Guide for Cosmetics Notification (2023), followed by a Claims Guide (EDREX:GL.CAPP.010), product-naming rules (reported effective 2025-01-01) and a variations-documents guide.Sources
- Market entry
- Mandatory pre-market notification on the EDA EgyCosm portal; a notification number is issued within 10 working days (3 days fast track) and is valid 10 years.
- Responsible person
- Notification is filed by an Egyptian company registered with the EDA (local manufacturer, importer or scientific office holding a brand-owner authorization letter).
- Safety file
- Composition form with INCI percentages, CoA, stability/shelf-life, Free Sale Certificate for imports, claim substantiation and clarification letters, with cosmetovigilance reporting within 20 days.
- Labeling
- Arabic mandatory (Arabic plus English artwork) showing product name, notification number/barcode, INCI list and usage instructions; advertising must be primarily Arabic.
- Animal testing
- No statutory ban identified.
- Ingredient lists
- EDA adopts the five EU 1223/2009 annexes (prohibited, restricted, colorants, preservatives, UV filters) plus EDA-specific limits.
- Mga Tala
- EDA PDFs/announcement pages could not be opened; guide dates are unverified. The 10-year notification validity comes from consultancy sources.
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Where this sits in the chain
Stage 6, QC & compliance: check ingredients against each market inventory first, read the market rules here once the formula is set, then run QC and the compliance file before shipping. ASEAN notification accounts have their own page.
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