← सभी बाज़ार

आधिकारिक निकाय

Food and Drug Administration (FDA Philippines), Center for Cosmetics Regulation and Research

प्रमुख नियमन

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

प्रभावी

2008-01-01

बाज़ार प्रवेश

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

जिम्मेदार व्यक्ति

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

सुरक्षा फ़ाइल

Product Information File per ACD Art. 8 under FDA Circular 2023-001, kept by the LTO holder for inspection.

लेबलिंग

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.

पशु परीक्षण

पंप बोतल 500ml

सामग्री सूची

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).

टिप्पणियाँ

ACD applied from 2008-01-01 while RA 9711 itself dates from 2009; notification validity (1–3 years) is from consultancy sources.

यहाँ इस इन्वेंटरी की खोज करें

东盟 · ASEAN Cosmetic Directive — Annexes

आधिकारिक पाठ

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/

स्रोत: 1234

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