Non-Prescription Drug Modernization Act of 2007
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Non-Prescription Drug Modernization Act of 2007 - Amends the Federal Food, Drug, and Cosmetic Act to authorize: (1) the amendment or repeal of an over-the-counter drug monograph without notice and public procedure if there is a finding by the Secretary of Health and Human Services that a category of drugs or a specific drug is associated with a significant risk or that such drugs lack evidence of effectiveness; and (2) the Food and Drug Administration (FDA) to regulate over-the-counter drug advertisements.
Directs the Commissioner of Food and Drugs to identify over-the-counter drug monographs that may require amendment or repeal and to report the findings to Congress.
Referred to the House Committee on Energy and Commerce.
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 4083: Non-Prescription Drug Modernization Act of 2007. 110th Congress. Open America. https://openamerica.io/bill/110-HR-4083/
"H.R. 4083: Non-Prescription Drug Modernization Act of 2007." 110th Congress, 2026, Open America, https://openamerica.io/bill/110-HR-4083/.
H.R. 4083, 110th Cong. (2026), https://openamerica.io/bill/110-HR-4083/.
[H.R. 4083: Non-Prescription Drug Modernization Act of 2007](https://openamerica.io/bill/110-HR-4083/)