Draft Guidance for Industry: Labeling of Dietary Supplements

The Food and Drug Administration (FDA) is announcing the availability of a revised draft guidance document entitled ``Draft Guidance for Industry: Questions and Answers Regarding the Labeling of Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act: Revision 1.'' This revised draft guidance is intended to assist the industry in complying with the labeling requirements prescribed for dietary supplement manufacturers, packers, and distributors by the Dietary Supplement and Nonprescription Drug Consumer Protection Act (the DSNDCPA).

The revised draft guidance changes the date on which FDA intends to begin enforcing these labeling requirements.