CFR Title 21 Parts 600 to 799 Food and Drugs Revised as of April 1, 2018

CFR Title 21 Parts 600 to 799|Code of Federal Regulations Title 21 Food and Drugs, 2018 Edition

Title 21—FOOD AND DRUGS is composed of nine volumes. The parts in these volumes are arranged in the following order: Parts 1–99, 100–169, 170–199, 200–299, 300–499, 500–599, 600–799, 800–1299 and 1300 to end. The first eight volumes, containing parts 1–1299, comprise Chapter I—Food and Drug Administration, Department of Health and Human Services. The ninth volume, containing part 1300 to end, includes Chapter II—Drug Enforcement Administration, Department of Justice, and Chapter III—Office of National Drug Control Policy. The contents of these volumes represent all current regulations codified under this title of the CFR as of April 1, 2018.

Table of Contents
Explanation ................................................................................................ v
Title 21:
Chapter I—Food and Drug Administration, Department of Health
and Human Services (Continued) ................................................. 3
Finding Aids:
Table of CFR Titles and Chapters ....................................................... 169
Alphabetical List of Agencies Appearing in the CFR ......................... 189
List of CFR Sections Affected ............................................................. 199

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES

Part Page
600 Biological products: general .................................... 5
601 Licensing ................................................................. 24
606 Current good manufacturing practice for blood and blood components ................................................. 45
607 Establishment registration and product listing for manufacturers of human blood and blood products and licensed devices ...................................... 59
610 General biological products standards .................... 66
630 Requirements for blood and blood components intended for transfusion or for further manufacturing use ............................................................. 84
640 Additional standards for human blood and blood products ............................................................... 94
660 Additional standards for diagnostic substances for laboratory tests .................................................... 117
680 Additional standards for miscellaneous products ... 134
SUBCHAPTER G—COSMETICS
700 General .................................................................... 137
701 Cosmetic labeling .................................................... 145
710 Voluntary registration of cosmetic product establishments.............................................................. 158
720 Voluntary filing of cosmetic product ingredient composition statements ....................................... 159
740 Cosmetic product warning statements .................... 163
741–799 [Reserved]

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