H.R. 1117 explained  ·  119th Congress  ·  Pending in Congress

Responsibility in Drug Advertising Act of 2025

Create a free account or sign in to follow H.R. 1117 and get alerts. Policy area: Health Create a free account or sign in to follow the Health policy area and get alerts. ▲ 619 days since action Sponsor: Rosa L. DeLauro, CT-03, D → Congress.gov

Cosponsors: none · per Congress.gov, 2026-10-12

Introduced: 2025-02-07

Latest action (2025-02-07): Referred to the House Committee on Energy and Commerce.

What H.R. 1117 does, in plain terms

Responsibility in Drug Advertising Act of 2025 This bill prohibits direct-to-consumer advertising of new drugs during the first three years following their approval by the Food and Drug Administration (FDA). Direct-to-consumer advertising includes advertising via social media. Upon request from a drug’s sponsor, the FDA may waive the prohibition during the third year following a drug’s approval if it determines that the direct-to-consumer advertising of the drug would have an affirmative value to public health. Conversely, the FDA may prohibit such advertising beyond the three-year period following approval if it determines that the drug has significant adverse health effects based on post-approval studies, adverse event reports, and other appropriate resources. The prohibition applies to new drugs approved beginning one year before the bill’s enactment.

Official summary by the Congressional Research Service, via Congress.gov.

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