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

  1. AM YA FENG QUIKE COMPOUND
    PARACETAMOL AND AMANTADINE
    HYDROCHLORIDE CAPSULES
  2. RYUKAKUSAN DIRECT
  3. CORIX BURNSGEL
  4.  OTC SOUTH OCEAN RIDACHE® SHEXIANG
    QUTONG QIWUJI
  5.  GMP ROSMARINUS SCHNEISKI
  6. MUHI
  7. TON PHOR SCAR OIL CROCCO
  8. MUHI MOPIDICKS®-S
  9. NEW SMELL LESS AMMELTZ® YOKOYOKO
  10. 180 [Label in Foreign Language]
  11. RYUKAKU-SAN FOR PHLEGM, COUGH,
    HUSKINESS
  12. PEPPERMINT CURE ORIGINAL RICQLES
    [as reflected in the secondary packaging]
    ALCOOL DE MINTHE DE RICQLES [as reflected in
    the primary packaging]

FDA Post-Marketing Surveillance (PMS) activities have verified that the abovementioned drug products have not gone through the registration and testing 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 their quality and safety. The consumption of such violative products may pose potential danger or injury if administered.

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.

In light of the above, the public is advised not to purchase the aforementioned violative products and to be vigilant against it. Always check if a drug product has been registered with the FDA before purchasing it by making use of the embedded Search feature of the FDA website accessible at www.fda.gov.ph. You may also look for the FDA Registration number on the product label.

All concerned establishments and/or entities are warned not to distribute the aboveidentified 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 [email protected] To report continuous sale or distribution of unregistered health products, kindly e-mail us via [email protected], or through the online reporting facility, eReport, at www.fda.gov.ph/ereport. You may also call the Center for Drug Regulation and Research at telephone number (02)809-5596. For any suspected adverse drug reaction (ADR), report immediately to FDA through this link: www.fda.gov.ph/adr-reportnew and fill out all the required fields.

Dissemination of the information to all concerned is requested.

 Please see attachment for the photos:-> FDA Advisory No. 2019-395