Food, Drug, and Cosmetic Act of 1938

Food, Drug, and Cosmetic Act of 1938

The Federal Food, Drug, and Cosmetic Act of 1938 greatly increased both the FDA’s regulatory power and the scope of its attentions.  The law expanded the agency’s focus beyond fraud to encompass safety as well. Most importantly, the 1938 act was the first law to require the testing of drugs before they were sent to market. It also banned drugs that didn’t list all their active ingredients. The Food, Drug and Cosmetic Act expanded the FDA’s authority to cover all medical devices and all cosmetics (with the exception of soap), and provided stronger regulation over deceptive packaging for food containers. 

Commentary

US Capitol building

Darrel Issa’s Government Handover

January 05, 2011

Cry Wolf Quotes

The disastrous provisions of this bill could wreck the industry of pharmacy.

-
Bruce Philip, Counsel for the National Association of Retail Druggists,testimony to the Senate Committee on Commerce

Unlimited power entrusted to bureaucrats warps their judgment on the opinions they might have as normal citizens.

-
William L. Daley of the National Editorial Association warned.

While both we and our clients are in entire sympathy with the aims and purposes of the Tugwell Bill, we are all of one mind in our fears about such a sweeping grant of autocratic power being placed in the hands of any bureau or department of government.

-
An advertising executive that represented the proprietary industry.

The enactment of this legislation will mean a complete readjustment, if indeed the business of manufacturing and selling packaged medicines can be continued at all. This is very doubtful.

-
Proprietary Association chief H.B. Thompson, Senate Committee on Commerce.