Title 21

PART 801 SUBPART C

Subpart C - Labeling Requirements for Over-the-Counter Devices

• 21 U.S.C. 321, 331, 351, 352, 360d, 360i, 360j, 371, 374.
• 41 FR 6896, Feb. 13, 1976, unless otherwise noted.

21:8.0.1.1.2.3.1.1	SECTION 801.60	801.60 Principal display panel.
21:8.0.1.1.2.3.1.2	SECTION 801.61	801.61 Statement of identity.
21:8.0.1.1.2.3.1.3	SECTION 801.62	801.62 Declaration of net quantity of contents.
21:8.0.1.1.2.3.1.4	SECTION 801.63	801.63 Medical devices; warning statements for devices containing or manufactured with chlorofluorocarbons and other class I ozone-depleting substances.

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