# Over-The-Counter Human Drugs; Labeling Requirements; Final Rule; Technical Amendment
> **Food and Drug Administration** · Final rule; technical amendment. · Published 2000-01-03 · Effective 2000-01-03 · 65 FR 7
## Document
- **Document number:** 99-34040
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 65 FR 7
- **CFR reference:** 21 CFR 201
- **Publication date:** 2000-01-03
- **Effective date:** 2000-01-03
- **HHS docket:** Docket Nos. 98N-0337, 96N-0420, 95N-0259, 90P-0201
## Abstract

The Food and Drug Administration (FDA) is amending the regulation that established a standardized format and standardized content requirements for the labeling of over-the-counter (OTC) drug products, and is amending several related OTC drug product labeling regulations. This amendment corrects and conforms several aspects of the new labeling requirements to other regulatory provisions and eliminates unnecessary text from the new labeling regulation.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2000/01/03/99-34040/over-the-counter-human-drugs-labeling-requirements-final-rule-technical-amendment)
---
*AI Analytics · CC0 1.0*