Regulations.gov document

Draft Guidance for Industry on Labeling Over-the-Counter Human Drug Products; Questions…

Notice · FDA-2004-D-0437 · posted Jan 14, 2005

Key facts

Document ID FDA-2004-D-0437-0001
Title Draft Guidance for Industry on Labeling Over-the-Counter Human Drug Products; Questions and Answers; Availability
Document type Notice
Subtype Notice of Availability
Agency FDA
Docket FDA-2004-D-0437
Posted Jan 14, 2005
Comment period opens Jan 12, 2005
Comments due Mar 15, 2005

At a glance

  • None Pages
  • No Open for comment
  • None Public comments on this docket

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Regulations.gov documents

Regulations.gov holds the rulemaking and other documents federal agencies post for public comment. Only agency documents are published here; public submissions are not.

Source: Regulations.gov (U.S. General Services Administration eRulemaking Program) · Source date:

Browse all Regulations.gov documents