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United States · Bill · HR

H.R. 2117 (110th)

Health Freedom Protection Act

referredUnited States· United States Congress· EN

Introduced

2 May 2007

Last action

2 May 2007 · Introduced

Status

Referred to the Subcommittee on Commerce, Trade and Consumer Protection.

Sponsors

Rep. Paul, Ron [R-TX-22], Rep. Burton, Dan [R-IN-6], Rep. Shays, Christopher [R-CT-4], Rep. Bartlett, Roscoe G. [R-MD-6], JOHN DUNCAN, Rescom. Fortuno, Luis G. [R-PR-At Large], PETER DEFAZIO, Rep. Kuhl, John R. "Randy", Jr. [R-NY-29], Rep. Musgrave, Marilyn N. [R-CO-4], DANA ROHRABACHER

Subjects

Agriculture

Source updated

14 August 2025

Agriculture

Summary

Health Freedom Protection Act - Amends the Federal Food, Drug, and Cosmetic Act (FFDCA) to provide that a food or dietary supplement is not a drug solely because the label or labeling contains a claim to cure, mitigate, treat, or prevent disease. Prohibits the Secretary of Health and Human Services from: (1) restricting the reprinting and distribution or sale of any U.S. government publication or any accurate quotations of such a publication, including content concerning nutrients and disease treatment or prevention; or (2) construing the distribution or sale of, or accurate quotation from, such a publication in connection with the sale of a food or dietary supplement as evidence of an intent to sell that food or dietary supplement as a drug. Requires the Secretary to allow claims on food or nutrient labeling that characterize the relationship of a nutrient to the cure, mitigation, treatment, or prevention of a disease (with no more than a three-sentence disclaimer) unless the Secretary proves by clear and convincing evidence that: (1) there is no scientific evidence that supports the claim; and (2) the claim is inherently misleading and incapable of being rendered nonmisleading through the addition of a disclaimer. Authorizes the use of specified health claims on the label of all foods and dietary supplements, including claims related to saw palmetto, omega-3 fatty acids, glucosamine, and calcium. Allows a statement for a dietary supplement to include words that are recognized as signs or symptoms of disease so long as the statement does not include the name of a specific disease. Amends the Federal Trade Commission Act to exempt from being regulated as advertising: (1) government publications exempted from reprinting or distribution restrictions under FFDCA; or (2) accurate summaries of scientific publications. Places the burden of proof that an advertisement for a dietary supplement or ingredient is false and misleading on the Federal Trade Commission.

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Timeline

  1. 2 May 2007

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

  2. 2 May 2007

    Introduced

    Referred to the House Committee on Energy and Commerce.

    Source: IntroReferral

  3. 2 May 2007

    Introduced

    Sponsor introductory remarks on measure. (CR E925)

    Source: IntroReferral

  4. 2 May 2007

    Introduced

    Introduced in House

    Source: IntroReferral

  5. 2 May 2007

    Introduced

    Introduced in House

    Source: IntroReferral

Votes

No vote records are attached yet.

Versions

Documents

3 official files

Introduced in House (text)

View fileDownload file

Sponsors

Related records

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Sources

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