Dietary Supplement and Nonprescription Drug Consumer Protection Act (S. 3546)

Format:

Book

Government document

Author/Creator:

Library of Congress. Congressional Research Service

Language:

English

Subjects (All):

Death.

Drugs.

People with disabilities.

Physical Description:

1 online resource

Contained In:

ProQuest U.S. Congressional Research Digital Collection

Place of Publication:

[Place of publication not identified] [publisher not identified] 2006

Summary:

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

Notes:

CRS Report

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

Vendor supplied data

Other Format:

Microfiche version Library of Congress Congressional Research Service Dietary Supplement and Nonprescription Drug Consumer Protection Act (S 3546)

Publisher Number:

CRS-2006-DSP-0631

Access Restriction:

Restricted for use by site license