Dietary Supplement Information Act
Official title: To amend the Federal Food, Drug, and Cosmetic Act to require that manufacturers of dietary supplements register with the Food and Drug Administration, to requi… Show full official titleShow less
Official title: To amend the Federal Food, Drug, and Cosmetic Act to require that manufacturers of dietary supplements register with the Food and Drug Administration, to require the submission to such Administration of reports on adverse experiences regarding such supplements, and for other purposes.
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Referred to the Subcommittee on Health.
Requires any dietary supplement manufacturer, packer, or distributor to initially report to the Secretary any serious adverse reactions to a supplement, to investigate the reaction, and to report any additional information obtained to the Secretary. Sets forth additional requirements for manufacturers.
Grants the Secretary authority to enter and inspect any factory, warehouse, or establishment in which dietary supplements are manufactured, processed, packed, or held, for introduction into interstate, or to enter and inspect any vehicle being used to transport or hold such supplements in interstate commerce.
Deems a food (includes dietary supplements) misbranded if its label does not contain the toll-free telephone number, and the address of the Internet site, maintained by the Secretary for purposes of the medical product reporting program (MedWatch or any successor program).
- Introduced in House Formatted Text PDF
Cite this page
U.S. Congress. (2026). H.R. 3065: Dietary Supplement Information Act. 107th Congress. Open America. https://openamerica.io/bill/107-HR-3065/
"H.R. 3065: Dietary Supplement Information Act." 107th Congress, 2026, Open America, https://openamerica.io/bill/107-HR-3065/.
H.R. 3065, 107th Cong. (2026), https://openamerica.io/bill/107-HR-3065/.
[H.R. 3065: Dietary Supplement Information Act](https://openamerica.io/bill/107-HR-3065/)