21 CFR Part 330 - OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED

Authority:
21 U.S.C. 321, 351, 352, 353, 355, 360, 360fff-6, 371.
Source:
39 FR 11741, Mar. 29, 1974, unless otherwise noted.
Editorial Note:
Nomenclature changes to part 330 appear at 69 FR 13717, Mar. 24, 2004.

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.


United States Code

Title 21 published on 2015-12-03

The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR Part 330 after this date.

  • 2016-11-23; vol. 81 # 226 - Wednesday, November 23, 2016
    1. 81 FR 84465 - Food and Drug Administration Review and Action on Over-the-Counter Time and Extent Applications
      GPO FDSys XML | Text
      DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration
      Final rule.
      This rule is effective December 23, 2016.
      21 CFR Part 330