Misbranded Drugs

PROHIBITED CLAIMS IN FOOD PRODUCTS - nicolas and de vega law offices

Prohibited Claims in Food Product Labels under FDA Regulations and Philippine law

Purpose of the Law To protect the public against dishonest or misleading advertising or promotion, and to ensure that every consumer acquires sufficient knowledge to be an informed consumer, particularly in the choice of the consumer products that he or she wishes to purchase or consume, the Food and Drug Administration (“FDA”) issued Administrative Order […]

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What are the FDA Mandatory Label Information for Food Products?

Mandate of the Food and Drug Administration Republic Act No. 3720, or otherwise known as the Food, Drug, and Cosmetic Act, is the law creating the Food and Drug Administration (“FDA”), which is under the Office of the Secretary of the Department of Health. The FDA is tasked by law to prescribe standards, guidelines, and

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DRUG LABELING REQUIREMENTS OF FDA - nicolas and de vega law offices images

Drug Labeling Requirements of the Food and Drug Administration

Governing Regulation for Drug Labelling Requirements The primary sources of information for consumers are the labels and labeling materials, as they provide useful information such as those dealing with the safe and effective use of a drug product (e.g. indication(s), pharmacologic class and dosage), and information dealing with quality (e.g. manufacturing and expiration dates, registration

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