Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act

1 organizations filed 2 public comments on Questions and Answers Regarding the Labeling of Nonprescription Human Drug Products Marketed Without an Approved Application as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act, at the Food and Drug Administration. The comment window closed 2584d ago.

Abstract

Docket Status: OPEN

Commenters (1)

• Consumer Healthcare Products Associationtrade assoc.

  2 filings · confidence 97%