To amend the Federal Food, Drug, and Cosmetic Act to provide for expedited approval of priority nonprescription drugs, and for other purposes.

Robert E. Latta

Republican · OH · Representative

Source: Congress.gov · FEC

• Greg Landsman (D-OH-1)Original· 2026-07-20

Referred to the House Committee on Energy and Commerce.

2026-07-20

Source: Congress.gov

The proposal would speed up the approval process for over-the-counter medications that address serious health needs or offer significant advantages over existing treatments, allowing drugmakers to get these products to consumers faster. This would affect pharmaceutical companies developing nonprescription drugs and potentially benefit patients who need access to new over-the-counter remedies more quickly. The bill also includes other provisions related to drug regulation under federal food and drug laws.

AI-assisted summary generated from the official bill metadata (title, subjects, actions) sourced from Congress.gov. Cached and reviewed. Always verify against the official text linked below.

[Congressional Bills 119th Congress] [From the U.S. Government Publishing Office] [H.R. 9774 Introduced in House (IH)] <DOC> 119th CONGRESS 2d Session H. R. 9774 To amend the Federal Food, Drug, and Cosmetic Act to provide for expedited approval of priority nonprescription drugs, and for other purposes. _______________________________________________________________________ IN THE HOUSE OF REPRESENTATIVES July 20, 2026 Mr. Latta (for himself and Mr. Landsman) 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 provide for expedited approval of priority nonprescription drugs, and for other purposes. Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, SECTION 1. PRIORITY NONPRESCRIPTION DRUGS. (a) In General.--The Federal Food, Drug, and Cosmetic Act is amended by inserting after section 506L (21 U.S.C. 356l) the following: ``SEC. 506M. PRIORITY NONPRESCRIPTION DRUGS. ``(a) In General.-- ``(1) Designation.--The Secretary may, at the request of the sponsor of a nonprescription drug, designate as a priority nonprescription drug under this section a drug intended for nonprescription use that is subject to an application submitted (or to be submitted) under section 505(b), if the Secretary determines that the drug meets the criteria specified in subsection (d). ``(2) Nonprescription defined.--In this section, the term `nonprescription' means, with respect to a drug, that such drug is not subject to section 503(b)(1). ``(b) Request for Designation.--The sponsor of a drug subject to a pending application under section 505(b) for nonprescription use may request that the Secretary designate the drug as a priority nonprescription drug. ``(c) Designation.--Not later than 60 calendar days after the receipt of a request under subsection (b), the Secretary shall determine whether a drug meets the criteria for designation as a priority nonprescription drug under this section, and if so, make such designation. ``(d) Criteria.-- ``(1) Eligibility.--Except as provided in paragraph (2), a drug described in subsection (a) is eligible for designation as a priority nonprescription drug if-- ``(A) the drug is intended for a novel nonprescription indication that could provide a meaningful public health benefit; ``(B) the drug is a new molecular entity; or ``(C) the drug contains an active ingredient that has never been available in a nonprescription drug. ``(2) Exclusion.--A drug is not eligible for designation as a priority nonprescription drug if the drug is subject to a risk evaluation and mitigation strategy under section 505-1 or if the drug is a controlled substance (as defined in section 102 of the Controlled Substances Act). ``(e) Actions.--If the Secretary designates a drug as a priority nonprescription drug, the Secretary shall take such actions as are appropriate to facilitate the development of, and expedite the review of, an application or supplement to an application for such drug, which may include-- ``(1) holding meetings with the sponsor and the review team throughout the development of the drug; ``(2) providing timely advice to, and interactive communication with, the sponsor regarding the development of the drug to ensure that the development program to gather the nonclinical and clinical data necessary to demonstrate the inapplicability of the criteria described in section 503(b)(1) is as efficient as practicable; ``(3) involving senior managers and experienced review staff, as appropriate, in a collaborative, cross-disciplinary review; ``(4) assigning a cross-disciplinary project lead for the Food and Drug Administration team to facilitate an efficient review of the development program and to serve as a scientific liaison between the review team and the sponsor; and ``(5) taking steps to ensure that the design of any necessary nonclinical or clinical trials is as efficient as…

practicable, when scientifically appropriate, including reliance on real world evidence. ``(f) List of Conditions.-- ``(1) Establishment.--Not later than 18 months after the date of enactment of this section, the Secretary shall publish in the Federal Register a list of conditions for which a nonprescription drug, if developed for the condition, could provide meaningful public health benefit. ``(2) Public comment.--The Secretary shall provide a period of not less than 30 days for public comment on-- ``(A) the list under paragraph (1); and ``(B) any updates to such list.''. (b) Rule of Construction.--The amendment made by subsection (a) shall not be construed to alter the evidentiary standards or the information required for approval of a nonprescription drug under section 505 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355). (c) Report to Congress.--Not later than 4 years after the date of enactment of this Act, the Secretary of Health and Human Services shall submit to Congress a report containing-- (1) the number of nonprescription drugs for which a sponsor requested that the Secretary designate such a drug as a priority nonprescription drug under section 506M of the Federal Food, Drug, and Cosmetic Act, as added by subsection (a); (2) the number of nonprescription drugs for which the Secretary approved such request; (3) the number of priority nonprescription drugs (as designated under such section) for which the Secretary approved an application under section 505 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355); (4) an overview of the resources used to implement such section; and (5) any recommendation on further improvement on increasing over-the-counter drug approvals using a framework similar to the designation framework established in such section. (d) Sunset Date.--The authority provided to the Secretary of Health and Human Services under section 506M of the Federal Food, Drug, and Cosmetic Act, as added by subsection (a), shall cease to be effective September 30, 2032. <all>

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