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