FDA issues warning vs. purchase, use of unregistered products

The Food and Drug Administration (FDA) advises the public against the purchase and use of the following unregistered drug products:

1. Tong Ren Tan Niu Huang Jie Du Pian 0.6g Tablet
2. OTC Paracetamol, Caffeine and Aspirin Powder
3. OTC Tongren Wuji Baifeng Wan [as reflected in the package insert]
4. Minocin Minocycline Hydrochloride Capsule 100mg
5. OTC Loratadine Tablets- Lü Lei Ta Ding Pian [as reflected in the package insert]

FDA Post-Marketing Surveillance (PMS) have verified that the abovementioned drug products have not gone through the registration process of the Agency and have not been issued with proper authorization in the form of Certificate of Product Registration. Thus, the Agency cannot guarantee its quality, safety and efficacy. Therefore, consumption of such violative products may pose potential danger or injury to health.

Pursuant to Republic Act No. 9711, otherwise known as the “Food and Drug Administration Act of 2009”, the manufacture, importation, exportation, sale, offering for sale, distribution, transfer, promotion, advertising or sponsorship of health products without proper authorization from FDA is prohibited.

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FDA issues warning vs. purchase, use of unregistered products

All concerned establishments and/or entities are warned not to distribute the above-identified violative drug products until they have already been covered by the appropriate authorization, otherwise, regulatory actions and sanctions shall be strictly pursued.

All Local Government Units (LGUs) and Law Enforcement Agencies (LEAs) are requested to ensure that these products are not sold or made available in their localities or areas of jurisdiction.

For more information and inquiries, please e-mail us at info@fda.gov.ph. To report continuous sale or distribution of unregistered health products, kindly e-mail us via ereport@fda.gov.ph. You may also call the Center for Drug Regulation and Research at telephone number (02) 8809-5596. For any suspected adverse drug reaction (ADR), report immediately to FDA through this link: https://primaryreporting.who-umc.org/Reporting/Reporter?OrganizationID=PH and fill out all the required fields.

FDA also issued a warning against the purchase, use, and selling of OTC Miao Medicine Fushu Zhiyanggao.

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