Chapter 71 - COMMERCIAL FEED
- Section 71.1 - General provisions
- Section 71.2 - Definitions
- Section 71.3 - Label format
- Section 71.4 - Drug labeling
- Section 71.5 - Guaranteed analysis requirements
- Section 71.6 - Ingredient listing requirements
- Section 71.7 - Nonprotein nitrogen
- Section 71.8 - Drug and feed additives
- Section 71.9 - Adulterants
- Section 71.10 - Brand and product names
- Section 71.11 - Directions for use and precautionary statements
- Section 71.12 - Good manufacturing practices