Federal Food, Drug, and Cosmetic Act

Federal Food, Drug, and Cosmetic Act (FD&C Act) is a comprehensive set of laws passed by the United States Congress in 1938 which gives authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics. The act was signed into law by President Franklin D. Roosevelt on June 25, 1938, and has been amended several times to include new standards for the safety and efficacy of products regulated by the FDA.

Background

The FD&C Act was enacted in response to growing public safety demands following a tragic public health disaster in 1937 involving the drug Elixir Sulfanilamide, which had not been tested for toxicity and resulted in the deaths of over 100 people. This incident highlighted the need for more stringent regulatory controls over drugs and led to the replacement of the earlier Pure Food and Drug Act of 1906.

Key Provisions

The FD&C Act introduced a number of key provisions aimed at protecting consumers, including:

• Pre-market Approval for New Drugs: Manufacturers are required to prove to the FDA that a drug is safe and effective for its intended use before it can be marketed.
• Adulteration and Misbranding: The act prohibits the adulteration and misbranding of food, drugs, and cosmetics in interstate commerce.
• Safe Tolerances for Poisonous Ingredients: The act allows the FDA to set safe tolerances for poisonous substances in foods.
• Factory Inspections: The act authorizes the FDA to conduct inspections of manufacturing facilities to ensure compliance with regulations.
• Cosmetics and Medical Devices Regulation: The act also brought cosmetics and medical devices under regulatory control, requiring safety evidence for new devices and prohibiting harmful ingredients in cosmetics.

Amendments

Over the years, the FD&C Act has been amended several times to address new challenges and advancements in science and technology. Notable amendments include:

• Durham-Humphrey Amendment (1951): Distinguished between over-the-counter and prescription drugs.
• Kefauver-Harris Amendment (1962): Required drug manufacturers to provide proof of both safety and efficacy of their products.
• Medical Device Amendments (1976): Established a comprehensive system for the review and approval of medical devices.
• Dietary Supplement Health and Education Act (1994): Set specific labeling requirements and authorized health claims for dietary supplements.

Impact

The FD&C Act has had a profound impact on public health and safety in the United States. It has provided the FDA with the authority to regulate a wide range of products, ensuring that they are safe, effective, and accurately labeled. The act has also fostered public confidence in the food and drug supply, contributing to the health and well-being of consumers.

See Also

• Pure Food and Drug Act
• Elixir Sulfanilamide disaster
• U.S. Food and Drug Administration
• Kefauver-Harris Amendment
• Medical Device Amendments of 1976
• Dietary Supplement Health and Education Act of 1994

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