13 Parts Of The Dietary Supplement Health And Education Act

The dietary supplement health and education act of 1994 dshea is a 1994 statute of united states federal legislation which defines and regulates dietary supplements.

13 parts of the dietary supplement health and education act. Fda traditionally considered dietary supplements to be composed only of essential nutrients such as vitamins minerals and proteins. A vitamin a mineral an herb. Public policy nutrition practice and the evolving health care market policy editor. Dshea is the acronym for the dietary supplement health and education act of 1994.

The dietary supplement health and education act of 1994 which spells out regulations regarding the manufacture and sale of dietary supplements defines a dietary supplement as a product other than tobacco intended to supplement the diet that bears or contains one of more of the following dietary ingredients. In the united states dietary supplements are defined by the 1994 dietary supplement health and education act as products that are not used exclusively as food but are intended to be consumed in addition to an individual s diet. However with passage of the dietary supplement health and education act of 1994 dshea congress amended the fd c act to include several provisions that apply only to dietary supplements and dietary ingredients of dietary supplements. Cosmetic act fd c act.

Glade phd cns facn from e c r 1 plymouth meeting pennsylvania usa the dietary supplement health and. The law provides fda with appropriate regulatory authority and ample enforcement tools to protect consumers while still allowing them the desired access to a wide variety of affordable high quality safe and beneficial dietary supplement products. Learn vocabulary terms and more with flashcards games and other study tools. This act may be cited as the dietary supplement health and education act of 1994.

As a result of these provisions dietary ingredients used in dietary. 11 12 1997 the dietary supplement health and education act of 1994 focus on labeling issues michael j. Under the act supplements are effectively regulated by the fda for good manufacturing practices under 21 cfr part 111. Whenever in this act an amendment or repeal is expressed in terms of an amendment to or repeal of a section or other provision the reference shall be considered to be made to a section or other provision of the federal food drug and cosmetic act.