Federal Food, Drug, and Cosmetic Act

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The United States Federal Food, Drug, and Cosmetic Act (FD&C) is a set of laws passed by Congress in 1938 giving authority to the Food and Drug Administration (FDA) to oversee the safety of food, drugs, and cosmetics. In 1968, the Electronic Product Radiation Control provisions were added to the FD&C. Also in that year the FDA formed the Drug Efficacy Study Implementation (DESI) to incorporate into FD&C regulations the recommendations from a National Academy of Sciences investigation of effectiveness of previously marketed drugs.[1] The act was amended by the FDA Modernization Act of 1997.

The introduction of this act was influenced by the death of more than 100 children. Elixir Sulfanilamide had been known to be a safe drug in powder and pill form. Its parent company dissolved it in diethylene glycol for sale in liquid form, but diethylene glycol (otherwise known as antifreeze) is highly toxic to the human body, resulting in death for those who took the new medication.

Contents

[edit] Food coloring

The FD&C is perhaps best known by the consumer because of its use in the naming of food coloring additives, such as "FD&C Yellow No. 6." The Act made the certification of food color additives mandatory.

The FDA lists nine FD&C (Food, Drugs & Cosmetics) certified color additives for use in foods in the United States, plus numerous D&C (Drugs & Cosmetics) colorings allowed only in drugs or cosmetics. Color additives derived from natural sources, such as vegetables, minerals or animals, and man-made counterparts of natural derivatives, are exempt from certification. Both artificial and natural color additives are subject to rigorous standards of safety before their approval for use in foods.

[edit] Certifiable colors: (name/common name)

Name Common name Color Comment
FD&C Blue No. 1 Brilliant Blue FCF bright blue
FD&C Blue No. 2 Indigotine royal blue
FD&C Green No. 3 Fast Green FCF sea green
FD&C Red No. 3 Erythrosine cherry red
FD&C Red No. 40 Allura Red AC orange-red
FD&C Yellow No. 5 Tartrazine lemon yellow
FD&C Yellow No. 6 Sunset Yellow FCF orange
Orange B Restricted to specific uses
Citrus Red No.2 Restricted to specific uses

[edit] Food Additives

The FFDCA act requires producers of food additives to demonstrate to a reasonable certainty that no harm will result from the intended use of an additive. If the FDA finds an additive to be safe the agency issues a regulation specifying the conditions under which the additive may be safely used.

[edit] Definition of Food Additive

The definition of "food additive" is "any substance, the intended use of which results directly or indirectly, in its becoming a component or otherwise affecting the characteristics of food". However, excluded from the definition of "food additive" are substances that are generally recognized, among experts qualified by scientific training and experience to evaluate their safety, as having been adequately shown through scientific procedures (or, in the case of a substance used in food before January 1, 1958, through either scientific procedures or through experience based on common use in food) to be safe under the conditions of their intended use. This is the so called generally recognized as safe (GRAS) exemption.[2]

[edit] GM foods are regarded as containing food additives

These regulations apply to foods produced by genetic engineering and if the protein added to the food by the genetic engineering process is not "generally recognized as safe" then genetically modified food is regarded as containing a "food additive" and is subject to pre-market approval by the FDA [3]. All GM foods sold in the USA have been subject to this FDA pre-market approval process.

[edit] Cosmetics

This Act defines cosmetics as products for "cleansing, beautifying, promoting attractiveness, or altering the appearance." In this sense the FDA can classify cosmetics without actually regulating them. This allows a manufacturer the ability to use ingredients or raw materials and market the final product without government approval. Questions are being raised about the potentially dangerous side effects of chemicals in everyday household products.

[edit] Related legislation

The Wheeler-Lea Act, also passed in 1938, granted the Federal Trade Commission the authority to oversee advertising of all products regulated by FDA, other than prescription drugs.

[edit] Significant amendments to FDCA and other laws related to FDCA

Amendments

  • Infant Formula Act of 1980, Public Law (PL) 96-359 (Oct. 26, 1980)
  • Orphan Drug Act, PL 97-414 (Jan. 4, 1983)
  • Drug Price Competition and Patent Term Restoration Act of 1984, PL 98-417 (Sept. 24, 1984)
  • Prescription Drug Marketing Act of 1987, PL 100-293 (Aug. 18, 1988)
  • Generic Animal Drug and Patent Term Restoration Act of 1988, PL 100-670 (Nov. 16, 1988)
  • Nutrition Labeling and Education Act of 1990, PL 101-535 (Nov. 8, 1990)
  • Safe Medical Devices Act of 1990, PL 101-629 (Nov. 28, 1990)
  • Medical Device Amendments of 1992, PL 102-300 (June 16, 1992)
  • Prescription Drug User Fee Act (PDUFA) of 1992, PL 102-571 (Oct. 29, 1992)
  • Animal Medicinal Drug Use Clarification Act (AMDUCA) of 1994, PL 103-396 (Oct. 22, 1994)
  • Dietary Supplement Health and Education Act of 1994, PL 103-417 (Oct. 25, 1994)
  • Food Quality Protection Act of 1996, PL 104-170 (Aug. 3, 1996)
  • Animal Drug Availability Act of 1996, PL 104-250 (Oct. 9, 1996)
  • Food and Drug Administration Modernization Act (FDAMA) of 1997, PL 105-115 (Nov. 21, 1997)
  • Best Pharmaceuticals for Children Act, PL 107-109 (Jan. 4, 2002)
  • Medical Device User Fee and Modernization Act (MDUFMA) of 2002, PL 107-250 (Oct. 26, 2002)
  • Animal Drug User Fee Act of 2003, PL 108-130 (Feb. 20, 2003)
  • Pediatric Research Equity Act of 2003, PL 108-155 (Dec. 3, 2003)
  • Minor Use and Minor Species Animal Health Act of 2004
  • Food Allergen Labeling and Consumer Protection Act of 2004, PL 108-282 (Aug. 2, 2004)

Other laws

  • Federal Food and Drugs Act of 1906 (repealed; for historical reference)
  • Federal Meat Inspection Act (March 4, 1907)
  • Federal Trade Commission Act (Sept. 26, 1914)
  • Filled Milk Act (March 4, 1923)
  • Import Milk Act (Feb. 15, 1927)
  • Public Health Service Act (July 1, 1944)
  • Trademark Act of 1946 (July 5, 1946)
  • Reorganization Plan 1 of 1953 (March 12, 1953)
  • Poultry Products Inspection Act (Aug. 28, 1957)
  • Fair Packaging and Labeling Act (Nov. 3, 1966)
  • The National Environmental Policy Act of 1969 (Jan. 1, 1970)
  • Controlled Substances Act (Oct. 27, 1970)
  • Controlled Substances Import and Export Act (Oct. 27, 1970)
  • Egg Products Inspection Act (Dec. 29, 1970)
  • Lead-Based Paint Poisoning Prevention Act (Jan. 13, 1971)
  • Federal Advisory Committee Act (Oct. 6, 1972)
  • Government in the Sunshine Act (Sept. 13, 1976)
  • Government Patent Policy Act of 1980 (Dec. 12, 1980)
  • Federal Anti-Tampering Act (Oct. 13, 1983)
  • Sanitary Food Transportation Act (Nov. 3, 1990)
  • Mammography Quality Standards Act (MQSA) (Oct. 27, 1992)
  • Bioterrorism Act of 2002 (June 12, 2002)
  • Project BioShield Act of 2004 (July 21, 2004)

[1]

[edit] See also

[edit] References

  1. ^ http://www.fda.gov/cder/about/history/time1.htm
  2. ^ http://www.cfsan.fda.gov/~lrd/fr970417.html
  3. ^ http://www.foodsafety.gov/~fsg/fssyst4.html

[edit] External links

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