21 CFR § 369.2 - Definitions.

---
identifier: "/us/cfr/t21/s369.2"
source: "ecfr"
legal_status: "authoritative_unofficial"
title: "21 CFR § 369.2 - Definitions."
title_number: 21
title_name: "Food and Drugs"
section_number: "369.2"
section_name: "Definitions."
chapter_name: "FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES"
subchapter_number: "D"
subchapter_name: "DRUGS FOR HUMAN USE"
part_number: "369"
part_name: "INTERPRETATIVE STATEMENTS RE WARNINGS ON DRUGS AND DEVICES FOR OVER-THE-COUNTER SALE"
positive_law: false
currency: "2026-04-05"
last_updated: "2026-04-05"
format_version: "1.1.0"
generator: "[email protected]"
authority: "21 U.S.C. 321, 351, 352, 353, 355, 360, 371."
regulatory_source: "39 FR 11745, Mar. 29, 1974, unless otherwise noted."
cfr_part: "369"
---


# 369.2 Definitions.

(a) As used in this part, the term *act* means the Federal Food, Drug, and Cosmetic Act.

(b) The terms *drugs* and *devices* are defined in section 201(g) and (k) of the act.

(c) Official compendia are defined in section 201(j) of the act.