Chapter 23 - ADULTERATED, MISBRANDED, OR NEW DRUGS AND DEVICES
- Section 39-23-10 - Short title
- Section 39-23-20 - Definitions
- Section 39-23-30 - Drug or device deemed adulterated
- Section 39-23-40 - Drug or device deemed misbranded
- Section 39-23-50 - Labeling or packaging requirements, exemptions; certain drugs must be dispensed only on prescription; requirements
- Section 39-23-55 - Labeling of prescription or nonprescription drug samples
- Section 39-23-60 - Coal-tar colors, regulations
- Section 39-23-70 - Intrastate commerce, introduction of new drugs
- Section 39-23-80 - Prohibited acts, penalties
- Section 39-23-100 - Procedure for condemnation of adulterated or misbranded drug or device
- Section 39-23-110 - Notice of criminal proceedings
- Section 39-23-120 - Minor violations of chapter
- Section 39-23-130 - Embargo of adulterated or misbranded drug or device