21 CFR Part 358 - MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE

Subpart A [Reserved]
Subpart B - Wart Remover Drug Products (§§ 358.101 - 358.150)
Subpart C [Reserved]
Subpart D - Ingrown Toenail Relief Drug Products (§§ 358.301 - 358.350)
Subpart E [Reserved]
Subpart F - Corn and Callus Remover Drug Products (§§ 358.501 - 358.550)
Subpart G - Pediculicide Drug Products (§§ 358.601 - 358.650)
Subpart H - Drug Products for the Control of Dandruff, Seborrheic Dermatitis, and Psoriasis (§§ 358.701 - 358.760)

Authority:

21 U.S.C. 321, 351, 352, 353, 355, 360, 371.

Source:

55 FR 33255, Aug. 14, 1990, unless otherwise noted.

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

U.S. Code: Title 21 - FOOD AND DRUGS

§ 321 - Definitions; generally

§ 351 - Adulterated drugs and devices

§ 352 - Misbranded drugs and devices

§ 353 - Exemptions and consideration for certain drugs, devices, and biological products

§ 355 - New drugs

§ 360 - Registration of producers of drugs or devices

§ 371 - Regulations and hearings