This document outlines Republic Act 3720, which establishes the Food and Drug Administration of the Philippines to regulate foods, drugs, and cosmetics. It creates the FDA under the Department of Health to set quality standards, ensure safety, and enforce relevant laws. It defines prohibited acts around adulterated or misbranded products and establishes penalties for violations. The act also provides definitions and standards for foods, drugs, cosmetics and related products to protect public health.
This document outlines Republic Act 3720, which establishes the Food and Drug Administration of the Philippines to regulate foods, drugs, and cosmetics. It creates the FDA under the Department of Health to set quality standards, ensure safety, and enforce relevant laws. It defines prohibited acts around adulterated or misbranded products and establishes penalties for violations. The act also provides definitions and standards for foods, drugs, cosmetics and related products to protect public health.
This document outlines Republic Act 3720, which establishes the Food and Drug Administration of the Philippines to regulate foods, drugs, and cosmetics. It creates the FDA under the Department of Health to set quality standards, ensure safety, and enforce relevant laws. It defines prohibited acts around adulterated or misbranded products and establishes penalties for violations. The act also provides definitions and standards for foods, drugs, cosmetics and related products to protect public health.
This document outlines Republic Act 3720, which establishes the Food and Drug Administration of the Philippines to regulate foods, drugs, and cosmetics. It creates the FDA under the Department of Health to set quality standards, ensure safety, and enforce relevant laws. It defines prohibited acts around adulterated or misbranded products and establishes penalties for violations. The act also provides definitions and standards for foods, drugs, cosmetics and related products to protect public health.
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Republic Act 3720
Domingo, John Alfred Kyle T.
BSFT IV INTRODUCTION • AN ACT TO ENSURE THE SAFETY AND PURITY OF FOODS, DRUGS, AND COSMETICS BEING MADE AVAILABLE TO THE PUBLIC BY CREATING THE FOOD AND DRUG ADMINISTRATION WHICH SHALL ADMINISTER AND ENFORCE THE LAWS PERTAINING THERETO. R.A. 3720 CHAPTER I • Section 1. This Act shall be known as the "Food, Drug, and Cosmetic Act.“ CHAPTER II Declaration of Policy • Section 2. It is hereby declared the policy of the State to insure safe and good quality supply of food, drug and cosmetic, and to regulate the production, sale, and traffic of the same to protect the health of the people. • Section 3. In the implementation of the foregoing policy, the Government shall in accordance with the provisions of this Act: (a) Establish standards and quality measures for food, drug, and cosmetic. (b) Adopt measures to insure pure and safe supply of food, drug, and cosmetic in the country. CHAPTER III • Section 4. To carry out the provisions of this Act, there is hereby created an office to be called the Food and Drug Administration in the Department of Health. Said Administration shall be under the Office of the Secretary and shall have the following functions, powers and duties: CHAPTER III • Section 5. The Food and Drug Administration shall have the following Divisions: (a) Inspection and Licensing Division, which shall have charge of the inspection of food, drug, and cosmetic establishments engaged in their manufacture and sale. (b) Laboratory Division, which shall conduct all the tests, analyses and trials of products covered by this Act. CHAPTER IV Board of Food and Drug Inspection • Section 9. The Board of Food Inspection is hereby converted into the Board of Food and Drug Inspection which shall consist of: CHAPTER VI PROHIBITED ACTS • Section 11. The following acts and the causing thereof are hereby prohibited: (a) The manufacture, sale, offering for sale or transfer of any food, drug, device or cosmetic that is adulterated or misbranded. PENALTIES • Section 12. (a) Any person who violates any of the provisions of Section eleven hereof shall, upon conviction, be subject to imprisonment of not less than six months and one day, but not more than five years, or a fine of not less than one thousand pesos, or both such imprisonment and fine, in the discretion of the Court. CHAPTER VII • Definition and Standards for Food. ADULTERATED FOOD MISBRANDED FOOD Tolerances for Poisonous Ingredients in Food COAL-TAR COLOR FOR FOOD • Section 17. (a) Any poisonous or deleterious substance added to any food, shall be deemed to be unsafe except when such substance is required or cannot be avoided in its production or manufacture. NEW DRUGS • Section 21. (a) No person shall manufacture, sell, offer for the sale or transfer any new drug, unless an application filed pursuant to subsection (b) is effective with respect to such drug. CHAPTER IX Certification of Drugs containing Penicillin, Streptomycin, Chlortetracycline, Chloramphenicol or Bacitracin. • The Secretary, pursuant to regulations promulgated by him shall provide for the certification of batches of drugs composed wholly or partly of any kind of penicillin, streptomycin, chlortetracycline, chloramphenicol, bacitracin, or any anti-biotic drug, or any derivative thereof. A batch of such drug shall be certified if such drug has such characteristics of identity, strength, quality and purity, as the Secretary prescribes in such regulations as necessary to adequately insure safety and efficacy of use, but shall not otherwise be certified. CHAPTER X ADULTERATED COSMETICS • Section 23. A cosmetic shall be deemed to be adulterated: (a) If it bears or contains any poisonous or deleterious substances which may render it injurious to users under the conditions of use prescribed in the labeling thereof, or under the conditions of use as are customary or usual: Provided, That this provision shall not apply to coal-tar hair dye, the label of which bears the following legend conspicuous displayed thereon: "Caution: This product contains ingredients which may cause skin irritation on certain individuals and a preliminary test according to accompanying directions should first be made. REGULATIONS MAKING EXEMPTIONS • Section 25. The Secretary shall promulgate regulations exempting from any labeling requirements of this Act cosmetic which are, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantities at establishments other than those where originally processed or packed, on condition that such cosmetics are not adulterated or misbranded under the provisions of this Act upon removal from such processing, labeling, repacking establishment. CHAPTER XI • General Administration Provisions, Regulations, Hearings and Institution of Criminal Action • Section 26. (a) Except as otherwise provided in this section, the Secretary of Health shall, upon recommendation of the Food and Drug Administrator, issue rules and regulations as may be necessary to enforce effectively the provisions of this Act.