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United States · Bill · S

S. 722 (108th)

Dietary Supplement Safety Act of 2003

openUnited States· United States Congress· EN

Introduced

26 March 2003

Last action

Status

Sponsor introductory remarks on measure. (CR S3547-3548)

Sponsors

Subjects

Discovery layer

Source updated

18 August 2025

Summary

Amends the Federal Food, Drug, and Cosmetic Act to require each manufacturer of a dietary supplement (supplement), and each packer or distributor of a supplement the name of which appears on the labeling, to report serious adverse experiences to the Secretary of Health and Human Services and to investigate such occurrences. Defines a serious adverse experience as an adverse event associated with the use of a supplement in a human that involves death or one of other serious calamities. Directs the Secretary to conduct a clinical evaluation of each such reported experience. Requires the manufacturer of a dietary supplement to report periodically on other adverse experiences and to review such occurrences. Allows the Secretary to grant a waiver from the above reporting, reviewing, and investigating requirements with respect to a dietary supplement upon determination that compliance is not necessary to protect the public health. Authorizes the Secretary to require a manufacturer to conduct postmarket surveillance for a supplement under specified circumstances. Permits the Secretary to require a manufacturer of a supplement or of an ingredient in a supplement to demonstrate that its product is safe under specified circumstances. Directs the Secretary to approve the continued marketing of such a supplement or ingredient or to disapprove it. Prohibits any introduction into interstate commerce of a supplement containing a stimulant unless it is approved by the Secretary under this Act. Amends the Act to exclude a product that bears or contains an anabolic steroid from the definition of a dietary supplement for a specified chapter of the Act. Eliminates a provision of the Act requiring the United States to bear the burden of proof to show a supplement or an ingredient in a supplement is adulterated due to a safety violation.

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3 official files

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