Food, Drug, and Cosmetics Acts of 1938, 1954, 1958 - PowerPoint PPT Presentation

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Food, Drug, and Cosmetics Acts of 1938, 1954, 1958

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Title: Food, Drug, and Cosmetics Acts of 1938, 1954, 1958


1
Food, Drug, and Cosmetics Acts of 1938, 1954, 1958
  • By Carly Mackay

2
This act was created to protect consumers from
harmful products in the drugs, food, and
cosmetics they bought
  • Gave the Food and Drug administration the
    power to oversee the safety of food, drugs, and
    cosmetics

3
  • Presented to Franklin Roosevelt by Congress he
    signed it on June 25, 1938
  • Replaced the 1906 Food and drugs act which was
    weakly enforced
  • 1954 Pesticides Amendment (set limits for
    pesticide residue on agricultural goods)
  • 1958 Food Additives Amendment (required FDA
    approval of any food additive found to cause
    cancer in humans or animals)

4
  • The American Chamber of Horrors The list of
    products that were not included in the 1906
    version of this law. They included
  • Banbar, a worthless "cure" for diabetes that the
    old law protected
  • Lash-Lure, an eyelash dye that blinded some women
  • Numerous examples of foods deceptively packaged
    or labeled
  • Radithor, a radium-containing tonic that
    sentenced users to a slow and painful death
  • The Wilhide Exhaler, which falsely promised to
    cure tuberculosis and other pulmonary diseases
  • This legislative act was finally brought to the
    publics attention when a drug company marketed
    Elixir Sulfanilamide, which contained a deadly
    chemical similar to antifreeze. Over 100 people
    died after using this product that was untested.

According to, http//www.fda.gov/oc/history/histo
ryoffda/section2.html
5
Goals of The FDCA
  • 1. Protect the publics safety -
  • The FDA ensures safety through inspections
    of products already on the market, controls the
    manufacturing practices of companies, and
    possesses recall and seizure authority.
  • according to http//www.answers.com/topic
    /federal-food-drug-and-cosmetic-act
  • 2. To reveal information to consumers -
  • The FDA outlaws misbranding and incorrect
    product labeling and requires some information on
    product labels like
  • The nutritional content box
  • Possible side effects and drug interactions
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