Introduced
Committee
Markup
Reported
Floor
Passed
Enacted
HR.7366 119th Congress

Dietary Supplement Regulatory Uniformity Act

Status
In Committee
Latest Action
2026-02-04
Sponsor
Official Source
Investability
0/100
Stage
COMMITTEE
Related Bills
0
Full Text
1,838 chars
Alive
Yes
Summary
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2026-02-04
Referred to the House Committee on Energy and Commerce.
2026-02-04
Introduced in House
2026-02-04
Introduced in House
119 HR 7366 IH: Dietary Supplement Regulatory Uniformity Act U.S. House of Representatives 2026-02-04 text/xml EN Pursuant to Title 17 Section 105 of the United States Code, this file is not subject to copyright protection and is in the public domain. I 119th CONGRESS 2d Session H. R. 7366 IN THE HOUSE OF REPRESENTATIVES February 4, 2026 Mr. Langworthy introduced the following bill; which was referred to the Committee on Energy and Commerce A BILL To amend the Federal Food, Drug, and Cosmetic Act to clarify and affirm the preemptive authority of the Food and Drug Administration over dietary supplement regulation, and for other purposes. 1. Short title This Act may be cited as the Dietary Supplement Regulatory Uniformity Act . 2. Clarification of Federal preemption with respect to dietary supplement regulation Section 403A of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 343–1 ) is amended by adding at the end the following: (c) (1) No State (or political subdivision thereof) may establish or continue in effect any requirement concerning a dietary supplement which is different from, or in addition to, or that is not otherwise identical with, a requirement applicable to a dietary supplement under this Act. (2) Upon application of a State or a political subdivision thereof, the Secretary may, by regulation and after notice and opportunity for a hearing, exempt from paragraph (1), under such conditions as may be prescribed in such regulation, a requirement of such State or political subdivision applicable to a dietary supplement if— (A) such requirement is more stringent than the applicable requirement under Federal law; or (B) (i) such requirement addresses a compelling local condition; and (ii) compliance with such requirement does not render the dietary supplement out of compliance with Federal law. .
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