# Over-the-Counter Human Drugs; Labeling Requirements; Partial Extension of Compliance Dates
> **Food and Drug Administration** · Final rule; partial extension of compliance dates. · Published 2000-06-20 · Effective 2000-07-20 · 65 FR 38191
## Document
- **Document number:** 00-15427
- **Category:** other
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 65 FR 38191
- **CFR reference:** 21 CFR 201
- **Publication date:** 2000-06-20
- **Effective date:** 2000-07-20
- **HHS docket:** Docket Nos. 98N-0337, 96N-0420, 95N-0259, and 90P-0201
## Abstract

The Food and Drug Administration (FDA) is providing a partial extension of the compliance dates for its final rule that appeared in the Federal Register of March 17, 1999. The final rule established a standardized format and standardized content requirements for the labeling of over-the-counter (OTC) drug products. That final rule requires all OTC drug products to have the new, easy-to-read format and the revised labeling requirements within prescribed implementation periods. This partial extension provides 1 additional year for implementation for specific types of OTC drug products to be in compliance with the final rule.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2000/06/20/00-15427/over-the-counter-human-drugs-labeling-requirements-partial-extension-of-compliance-dates)
---
*AI Analytics · CC0 1.0*