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Southeast Asia · Philippines

What does it take to sell cosmetics in Philippines? Entry route, responsibility, labeling

Pre-market Cosmetic Product Notification via the FDA eServices portal (with PIF upload) b…; Responsible person: A Philippine company holding an FDA License to Operate (LTO…; Labeling: ACD Appendix I labelling in English or Filipino: ….

Latest change 2026-04-22 — FDA Circular No. 2026-0001 consolidated ACD amendments from the 40th–42nd ACC meetings, adding TMPTA to Annex II, amending the benzophenone entry (effective 2026-11-19) and restricting BHT with a 24-month grace period. Source

Factory-side digest; the official text prevails; not legal advice.

Authority
Food and Drug Administration (FDA Philippines), Center for Cosmetics Regulation and Research
Main regulation
RA 9711 (2009); AO 2005-0025; FDA Circular 2023-001 (PIF) · Republic Act No. 9711 (FDA Act of 2009) amending RA 3720, with the ASEAN Cosmetic Directive adopted by DOH Administrative Order No. 2005-0025
In force
2008-01-01
Market entry
Pre-market Cosmetic Product Notification via the FDA eServices portal (with PIF upload) before distribution, valid 1–3 years and renewable.
Responsible person
A Philippine company holding an FDA License to Operate (LTO) as manufacturer, importer or distributor must file the notification and appear on the label.
Safety file
Product Information File per ACD Art. 8 under FDA Circular 2023-001, kept by the LTO holder for inspection.
Labeling
ACD Appendix I labelling in English or Filipino: product name and function, full ingredient list, country of manufacture, LTO holder name/address, contents, batch, manufacturing/expiry date and precautions, with claims following the ACD claims guidelines.
Animal testing
No ban and no requirement.
Ingredient lists
ACD Annexes II–VII as adopted through FDA circulars (latest FDA Circular 2026-0001; FDA Circular 2025-002 of 2025-03-18 adopted the 39th ACC changes such as the DEET ban).
Notes
ACD applied from 2008-01-01 while RA 9711 itself dates from 2009; notification validity (1–3 years) is from consultancy sources.
Look up this inventory here
东盟 · ASEAN Cosmetic Directive — Annexes
Official text
https://www.fda.gov.ph/fda-circular-no-2026-0001-consolidated-amendments-to-the-asean-cosmetic-directive-acd-as-adopted-during-the-40th-to-42nd-asean-cosmetic-committee-acc-meeting-and-their-related-meetings/

FAQ

Does Philippines require notification or registration before sale?

Pre-market Cosmetic Product Notification via the FDA eServices portal (with PIF upload) before distribution, valid 1–3 years and renewable.

Is a local responsible person mandatory in Philippines?

A Philippine company holding an FDA License to Operate (LTO) as manufacturer, importer or distributor must file the notification and appear on the label.

What are the labeling requirements in Philippines?

ACD Appendix I labelling in English or Filipino: product name and function, full ingredient list, country of manufacture, LTO holder name/address, contents, batch, manufacturing/expiry date and precautions, with claims following the ACD claims guidelines.

What changed recently in Philippines cosmetic regulation?

2026-04-22 FDA Circular No. 2026-0001 consolidated ACD amendments from the 40th–42nd ACC meetings, adding TMPTA to Annex II, amending the benzophenone entry (effective 2026-11-19) and restricting BHT with a 24-month grace period.

Source: 1234

Manufacturing for Philippines · by category

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