Section 39-18-39 – Access of departmental personnel to premises.
39-18-39. Access of departmental personnel to premises. The secretary of agriculture and natural resources or his agent shall have free access at all reasonable hours to any establishment in which animal remedies are manufactured, processed, packed, sold, or offered for sale, to inspect such premises and to determine whether the provisions of this chapter are […]
Section 39-18-40 – Procurement and analysis of samples–Official analysis as sole guide for administrative determinations.
39-18-40. Procurement and analysis of samples–Official analysis as sole guide for administrative determinations. The secretary of agriculture and natural resources or his agent may secure samples or specimens of any animal remedy after paying or offering to pay for them, and he shall make an examination or analysis of such samples to determine whether the […]
Section 39-18-41 – Refusal of inspection or sample prohibited.
39-18-41. Refusal of inspection or sample prohibited. No person shall refuse to permit entry or inspection, or to permit the acquisition of a sample or specimen of an animal remedy, as authorized by §§39-18-39 and 39-18-40. Source: SL 1966, ch 8, §10 (e).
Section 39-18-42 – Analysis result showing adulteration or misbranding forwarded to distributor and purchaser–Portion of sample furnished.
39-18-42. Analysis result showing adulteration or misbranding forwarded to distributor and purchaser–Portion of sample furnished. When the inspection and analysis of an official sample indicates an animal remedy has been adulterated or misbranded, the results of analysis shall be forwarded by the secretary of agriculture and natural resources to the distributor and the purchaser. Upon […]
Section 39-18-43 – Unauthorized disclosure of information prohibited.
39-18-43. Unauthorized disclosure of information prohibited. The secretary of agriculture and natural resources or any of his agents shall not use or reveal information acquired under §§39-18-5, 39-18-6, and 39-18-38 to 39-18-40, inclusive, except in the enforcement of this chapter, or to the courts, when relevant. Source: SL 1966, ch 8, §10; SL 2021, ch […]
Section 39-18-29 – Substandard strength or quality as adulteration–Tolerance allowed.
39-18-29. Substandard strength or quality as adulteration–Tolerance allowed. An animal remedy shall be deemed to be adulterated if its composition, purity, strength, or quality falls below or differs from that which it is purported or is represented to possess by its labeling; but, the secretary of agriculture and natural resources shall allow a reasonable tolerance […]
Section 39-18-20 – Remedy deemed misbranded if required information on label not conspicuous and clear.
39-18-20. Remedy deemed misbranded if required information on label not conspicuous and clear. An animal remedy shall be deemed to be misbranded if any word, statement, or other information required to appear on the label is not prominently placed on such label with such conspicuousness, as compared with other words, statements, designs, or devices in […]
Section 39-18-21 – Remedy deemed misbranded if container deceptive as to quantity.
39-18-21. Remedy deemed misbranded if container deceptive as to quantity. An animal remedy shall be deemed to be misbranded if its container is so made, formed, or filled as to be deceptive or misleading as to the amount of contents. Source: SL 1966, ch 8, §7 (b).
Section 39-18-22 – Remedy deemed misbranded if distributed under name of another.
39-18-22. Remedy deemed misbranded if distributed under name of another. An animal remedy shall be deemed to be misbranded if it is distributed under the name of another animal remedy. Source: SL 1966, ch 8, §7 (d).
Section 39-18-23 – Remedy deemed misbranded if recommended dosage is dangerous.
39-18-23. Remedy deemed misbranded if recommended dosage is dangerous. An animal remedy shall be deemed to be misbranded if it is dangerous to the health of animals when used in the dosage or with the frequency or duration prescribed, recommended, or suggested in the labeling of such remedy. Source: SL 1966, ch 8, §7 (e).