Category: Food Announcements


Calling Company Representatives/ Regulatory Affairs Personnel/ Liaison Officers and/ or Company Owners of Food Business and other Stakeholders

The programs provide a procedural discussion on the licensing application process and regulatory requirements for food establishments.

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The Food and Drug Administration (FDA) requires two (2) types of authorizations before any processed food product can be released in the Philippine market. The first is the License-to- Operate (LTO) which is an authorization granted to manufacturers, repackers, importers, distributors, wholesalers, traders who passed FDA guidelines such as Good Manufacturing Practices. After being issued an LTO, the food business operator is required to secure another authorization which is called Certificate of Product Registration (CPR). The evaluation process for CPR entails checking of the safety and quality of a respective product with applicable standards and issuances.

These have been the basic requirements of FDA since 2009 with the passage of Republic Act No. 9711 or the FDA Act of 2009. On 28 December 2009, a joint issuance was issued by the Department of Agriculture (DA) and Department of Health (DOH) in transferring the mandate of regulation from DOH-FDA to DA-National Meat Inspection Service (NMIS) of processed meat products. The mandate only returned to the DOH-FDA with the signing of Republic Act No. 10611 or the Food Safety Act of 2013. The transfer was fully implemented on 01 May 2017, and FDA started requiring a valid CPR prior to the distribution of all processed meat, including liver spread products such as RENO Brand.

RENO Foods, Incorporated, the manufacturer of RENO brand Liver spread has an existing LTO as food repacker. In 2017, the company applied for the variation of their LTO to include their product line as manufacturer of processed meat products. Upon inspection of the FDA, the company was granted approval of the LTO as manufacturer. However, FDA inspectors instructed the company to secure CPRs for their products, including RENO Brand Liver Spread.

This year, FDA inspectors collected samples of RENO Brand Liver Spread for verification of their CPR. Upon extensive search of FDA databases, the mentioned liver spread failed to secure a CPR. Thus, the FDA has a responsibility to inform the public, through an advisory, that RENO Brand Liver Spread is NOT REGISTERED as of this date as a processed food product and must secure the required authorization from this Office.


FDA Advisory No. 2020-531 || Public Health Warning Against the Unapproved and Misleading Advertisement of Food Products and Food Supplements Claiming to Boost Immune System and Decrease the Risk for Coronavirus Disease (COVID)-19 Infection

The Food and Drug Administration (FDA) warns the public against unapproved and misleading advertisements and promotion of various food products and food supplements monitored online:

  1. Misleading advertisement of UNREGISTERED Honey-C Vitamin C Supplement
  2. Misleading Advertisement of GLUTA-WHITE and GLUTA-WHITE 500 Food Supplement Capsules (source:
  3. Misleading Advertisement of KINGS HERBAL Food Supplement Liquid (source:
  4. Misleading Advertisement of  ONE OPTI JUICE Herbal Proprietary Blend Powdered Juice (source:
  5. Misleading Advertisement of SANTE BARLEY Pure Barley Food Supplement Powder(source:

The public is hereby advised to be vigilant against such deceptive marketing of food products and food supplements. Food products and food supplements shall not, in any way, prevent, cure and especially reduce the risk of COVID-19 and any other diseases, and should not bear any misleading, deceptive, and false claims on their labels and/or any promotional materials that will provide erroneous impression on the product’s character or identity.

Further, the FDA would like to emphasize that of this time, there are no specific vaccines or treatments for COVID-19. Everyone is encouraged to follow accurate public health advice and guidance from the Department of Health and the World Health Organization on basic protective measures against COVID-19.

All Market Authorization Holders of these food products and food supplements are sternly warned and hereby directed to stop such misleading advertisements and promotions. Appropriate regulatory tools and sanctions shall be executed to such companies that are continuously conducting such and other similar activities upon issuance of this Advisory.

Dissemination of this advisory to all concerned is hereby requested.

Attachment:->FDA Advisory No.2020-531

/ In Food Announcements / By Administrator / Comments Off on FDA Advisory No. 2020-531 || Public Health Warning Against the Unapproved and Misleading Advertisement of Food Products and Food Supplements Claiming to Boost Immune System and Decrease the Risk for Coronavirus Disease (COVID)-19 Infection