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The Dietary Supplement Health and Education Act of 1994, a law that regulates the supplement industry in the United States.
Federal and state law combine to give consumers and regulators multiple tools against : the enforces truth-in-advertising and can demand refunds, corrective ads, injunctive relief, and bans, while the...
The FDA removes or compels correction of misbranded dietary supplements using a laddered mix of administrative notices, civil court actions (including injunctions), criminal prosecutions and financial...
The Dietary Supplement and Nonprescription Drug Consumer Protection Act requires the “responsible person” named on a U.S.-market label—typically the manufacturer, packer, or distributor—to provide a d...
There is no direct record in the provided reporting of a definitive 2014 U.S. Senate hearing conclusion specifically about physician endorsements of dietary supplements; the documents available instea...
The FDA does not pre-approve dietary supplements before they hit shelves; instead, the law places primary responsibility on manufacturers to ensure safety and labeling, and empowers FDA to act after p...
Consumers buying weight‑loss supplements should insist on complete, transparent ingredient lists on a Supplement Facts panel and independent third‑party certification that verifies label accuracy and ...
The federal framework that governs dietary supplements remains rooted in DSHEA, which leaves most products subject to post‑market enforcement rather than pre‑market approval . Since 2014 regulators an...
Federal and state consumer-protection tools exist to punish and remedy deceptive celebrity or “doctor” endorsements for online supplements: the Federal Trade Commission enforces truth-in-advertising r...
Regulatory oversight of celebrity-linked tinnitus supplements sits at the crossroads of a permissive supplement law and active advertising rules: the FDA oversees safety and labeling but rarely pre-sc...