Latest Advisory

  • FDA Advisory No. 2017-319 || Public Health Warning Against the Purchase and Consumption of Unregistered and Unfortified Flour Products

    FDA Advisory No. 2017-319 || Public Health Warning Against the Purchase and Consumption of Unregistered and Unfortified Flour Products

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  • FDA Advisory No. 2017-316 || Public Health Warning Against the Purchase and Consumption   of the following Unregistered and Unfortified Food Oil  Products:

    FDA Advisory No. 2017-316 || Public Health Warning Against the Purchase and Consumption of the following Unregistered and Unfortified Food Oil Products:

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  • FDA Advisory No. 2017-318 || Suspension of Sale/Marketing/Distribution of Sanofi Pasteur, Inc.’s Tetravalent Vaccine (Live, Attenuated)(Dengvaxia)

    FDA Advisory No. 2017-318 || Suspension of Sale/Marketing/Distribution of Sanofi Pasteur, Inc.’s Tetravalent Vaccine (Live, Attenuated)(Dengvaxia)

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  • FDA Advisory No. 2017-317 || ACCEPTANCE OF ALL APPLICATIONS AT THE FOOD AND DRUG ACTION CENTER (FDAC) CASHIER

    FDA Advisory No. 2017-317 || ACCEPTANCE OF ALL APPLICATIONS AT THE FOOD AND DRUG ACTION CENTER (FDAC) CASHIER

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  • FDA Advisory No. 2017-315 || Voluntary Recall of BD Vacutainer K2 EDTA (K2E) 3.6mg Blood Collection Tube, 13 x 75mm x 2.0mL

    FDA Advisory No. 2017-315 || Voluntary Recall of BD Vacutainer K2 EDTA (K2E) 3.6mg Blood Collection Tube, 13 x 75mm x 2.0mL

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  • FDA Advisory No. 2017-314 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 67)

    FDA Advisory No. 2017-314 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 67)

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  • FDA Advisory No. 2017-313 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 13)

    FDA Advisory No. 2017-313 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 13)

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  • FDA Advisory No. 2017-312 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 12)

    FDA Advisory No. 2017-312 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 12)

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  • FDA Advisory No. 2017-311 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

    FDA Advisory No. 2017-311 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

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  • FDA Advisory No. 2017-310 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

    FDA Advisory No. 2017-310 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

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  • FDA Advisory No. 2017-309 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

    FDA Advisory No. 2017-309 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Supplements:

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  • FDA Advisory No. 2017-308 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

    FDA Advisory No. 2017-308 || Public Health Warning Against the Purchase and Consumption of the following Unregistered Food Products:

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  • FDA Advisory No. 2017-307 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 63)

    FDA Advisory No. 2017-307 || Public Health Warning Against the Use of Unnotified Cosmetic Products (Batch 63)

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  • FDA Advisory No. 2017-306 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 11)

    FDA Advisory No. 2017-306 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 11)

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  • FDA Advisory No. 2017-305 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 10)

    FDA Advisory No. 2017-305 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 10)

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  • FDA Advisory No. 2017-304 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 9)

    FDA Advisory No. 2017-304 || Public Health Warning Against the Use of Counterfeit Cosmetic Products (Batch 9)

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  • FDA Advisory No. 2017-303 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Supplements Claiming to Contain L-Glutathione:

    FDA Advisory No. 2017-303 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Supplements Claiming to Contain L-Glutathione:

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  • FDA Advisory No. 2017-297 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Products and Food Supplements:

    FDA Advisory No. 2017-297 || Public Health Warning Against the Purchase and Consumption of the Following Unregistered Food Products and Food Supplements:

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  • FDA Advisory No. 2017-299 || Public Health Warning Against the Use of Unregistered Household/Urban Pesticide Products (Batch 19)

    FDA Advisory No. 2017-299 || Public Health Warning Against the Use of Unregistered Household/Urban Pesticide Products (Batch 19)

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  • FDA Advisory No. 2017- 296 || Public Health Warning Against the Use of Unnotified Toy and Childcare Article (TCCAs) Products (Batch 11)

    FDA Advisory No. 2017- 296 || Public Health Warning Against the Use of Unnotified Toy and Childcare Article (TCCAs) Products (Batch 11)

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Administrative Order No. 2016-0008

Revised Rules and Regulations Governing the Generic Labeling Requirements of Drug Products for Human Use

I. RATIONALE

Article III, Section 7 of the 1987 Philippines Constitution declares that the state recognizes the right of the people to gain information on matters of public concern, such as those relating to health and health products.

 

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Administrative Order 2016-0003

Guidelines on the Unified Licensing Requirements and Procedure of the Food and Drug Administration (FDA)

I. RATIONALE

The 1987 Philippine Constitution mandates the establishment of an effective food and drug regulatory system that is responsive to the country's health needs and problems.

Consistent with said constitutional provision, Congress passed landmark legislations, namely Republic Act (RA) No. 3720 (Food, Drugs and Devices and Cosmetics Act), as amended by RA No. 9711 (Food and Drug Administration Act of 2009), RA No. 10611 (Food Safety Act of 2013), and RA No. 9502 Universally Accessible Cheaper and Quality Medicine Act of 2008) mandating FDA to regulate establishments engaged in health products to ensure consumer safety, welfare protection, and fair practice

 

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