41 chapters · 628 sections in this title.
S.C. Code Ann. § 39-23-40 Drug or device deemed misbranded
8.6K chars
A drug or device shall be deemed to be misbranded: (a) If its label is false or misleading in any particular. (b) If in a package form unless it bears a label containing (1) the name and place of business of the manufacturer, packer, or distributor; and (2) an accurate statement …
S.C. Code Ann. § 39-23-50 Labeling or packaging requirements, exemptions; certain drugs must be dispensed only on prescription; requirements
3.8K chars
(a) The Director of Health and Environmental Control is hereby directed to promulgate regulations exempting from any labeling or packaging requirement of this chapter drugs and devices which are, in accordance with the practice of the trade, to be processed, labeled, or repacked …
S.C. Code Ann. § 39-23-55 Labeling of prescription or nonprescription drug samples
0.9K chars
(A) For purposes of this section, "sample" means a unit of a drug which is not intended by the manufacturer to be sold and which is intended to promote the sale of the drug. (B) The department may not require the labeling of a prescription or nonprescription drug sample for which…
S.C. Code Ann. § 39-23-60 Coal-tar colors, regulations
0.3K chars
In accordance with Federal standards, the Director of Health and Environmental Control shall promulgate regulations providing for the listing of coal-tar colors which are harmless and suitable for use in drugs for purposes of coloring only and for the certification of batches of …