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Dietary Supplement and Nonprescription Drug Consumer Protection Act (S. 3546)
Summarizes provisions of S. 3546, the Dietary Supplement and Nonprescription Drug Consumer Protection Act of 2006, to require manufacturers of dietary supplements and over-the-counter drugs to report serious adverse events to the FDA, including deaths, birth defects, hospitalizations, incapacitations, or life-threatening experiences resulting from the use of nonprescription drugs or supplements.
Record is based on bibliographic data in ProQuest U.S. Congressional Research Digital Collection (last viewed Dec. 2010). Reuse except for individual research requires license from ProQuest, LLC.
Library of Congress. Congressional Research Service.