Labeling
---
identifier: "/us/fr/03-55525"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Labeling"
title_number: 0
title_name: "Federal Register"
section_number: "03-55525"
section_name: "Labeling"
positive_law: false
currency: "2003-09-29"
last_updated: "2003-09-29"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "03-55525"
document_type: "rule"
publication_date: "2003-09-29"
agencies:
- "Health and Human Services Department"
- "Food and Drug Administration"
cfr_references:
- "21 CFR Part 201"
fr_citation: "68 FR 55822"
fr_volume: 68
---
# Labeling
**CFR Correction**
In Title 21 of the Code of Federal Regulations, parts 200 to 299, revised as of April 1, 2003, in the first sentence of the introductory text of § 201.122, on page 54, the phrase “ ‘Rx only’ ” is removed and the phrase “ ‘Caution: For manufacturing, processing, or repacking’ ” is added in its place, and the phrase “ ‘Caution: Federal law prohibits dispensing without prescription’ ” is removed and the phrase “ ‘Rx only’ ” is added in its place.