South Dakota Codified Laws
Chapter 18 - Animal Remedies
Section 39-18-1 - Definition of terms.

39-18-1. Definition of terms.
Terms used in this chapter mean:
(1)"Advertisement," all representations, other than those on the label, disseminated in any manner or by any means, relating to animal remedies as defined in this chapter;
(2)"Animal," any animate being, which is not human, endowed with the power of voluntary action;
(3)"Animal remedies," all drugs, combination of drugs, proprietary medicines, biological products, and combinations of drugs and other ingredients, other than for food or cosmetic purposes, which are prepared or compounded for animal use; except those exempted by the secretary of agriculture and natural resources;
(4)"Brand name," any word, name, symbol, or device, or any combination thereof, identifying the animal remedy of a distributor and distinguishing it from that of others;
(5)"Distribute," to offer for sale, sell, or barter;
(6)"Dosage form," any animal remedy prepared in tablets, pills, capsules, ampules, or other units suitable for administration as an animal remedy;
(7)"Drug,":
(a)Articles recognized in the official United States Pharmacopoeia, the official Homeopathic Pharmacopoeia of the United States, official National Formulary, or any supplement to any of them;
(b)Articles intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease in animals;
(c)Preparations for external or internal use in the mitigation of parasites in or on animals;
(d)Articles (other than food) intended to affect the structure or any function of the body of animals;
(e)Articles intended for use as a component of any articles specified in subsection (a), (b), (c), or (d) of this subdivision;
but does not include devices or their components, parts, or accessories;
(8)"Label," a display of written, printed, or graphic matter upon the immediate container of any article; and a requirement made by or under authority of this chapter that any word, statement, or other information appearing on the label may not be considered to be complied with unless such word, statement, or other information also appears on the outside container or wrapper, if any there be, of the retail package of such article, or is easily legible through the outside container or wrapper;
(9)"Labeling," all labels and other written, printed, graphic matter:
(a)Upon any article or any of its containers or wrappers;
(b)Accompanying such article;
(10)"Person," any individual, firm, partnership, limited liability company, corporation, association, or organized group of persons whether incorporated or not;
(11)"Product name," the name of the animal remedy which identifies it as to kind, class, or specific use.

Source: SL 1913, ch 332; RC 1919, §7892; SL 1929, ch 238, §1; SDC 1939, §22.1002; SL 1964, ch 6, §2; SL 1966, ch 8, §3; SL 1994, ch 351, §95; SL 2021, ch 1 (Ex. Ord. 21-3), § 14, eff. Apr. 19, 2021.

Structure South Dakota Codified Laws

South Dakota Codified Laws

Title 39 - Food and Drugs

Chapter 18 - Animal Remedies

Section 39-18-1 - Definition of terms.

Section 39-18-2 - Administration of chapter.

Section 39-18-3 - Registration required for distribution of remedy.

Section 39-18-4 - Experimental remedies exempt from registration--Labeling.

Section 39-18-5 - Application for registration--Contents.

Section 39-18-6 - Label to accompany application--Specimen required--Statement of claims.

Section 39-18-7 - Classification by secretary as commercial feed or animal remedy.

Section 39-18-8 - Copy of registration forwarded to applicant_Annual expiration date.

Section 39-18-9 - Disposition of funds collected.

Section 39-18-10 - Refusal to register product of no value--Suspension or revocation for flagrant violation.

Section 39-18-11 - No additional fee required if paid by manufacturer or distributor.

Section 39-18-12 - Sale or offer of unregistered remedy prohibited.

Section 39-18-13 - Sale by retailer without reregistration.

Section 39-18-14 - Professional supervision required for preparation and packaging of remedies.

Section 39-18-15 - Label required on animal remedy--Contents.

Section 39-18-16 - Forgery or counterfeiting of label prohibited.

Section 39-18-17 - Alteration or destruction of label prohibited--Other acts resulting in misbranding.

Section 39-18-18 - Remedy deemed misbranded if not properly labeled.

Section 39-18-19 - Remedy deemed misbranded if label misleading.

Section 39-18-20 - Remedy deemed misbranded if required information on label not conspicuous and clear.

Section 39-18-21 - Remedy deemed misbranded if container deceptive as to quantity.

Section 39-18-22 - Remedy deemed misbranded if distributed under name of another.

Section 39-18-23 - Remedy deemed misbranded if recommended dosage is dangerous.

Section 39-18-24 - Distribution under federal license as compliance with branding requirements.

Section 39-18-25 - Putrid and decomposed substances constituting adulteration.

Section 39-18-26 - Poisonous and deleterious substances constituting adulteration.

Section 39-18-27 - Injurious substance in container constituting adulteration.

Section 39-18-28 - Preparation or packing under unsanitary conditions as adulteration.

Section 39-18-29 - Substandard strength or quality as adulteration--Tolerance allowed.

Section 39-18-30 - Manufacture or sale of adulterated or misbranded remedy prohibited.

Section 39-18-31 - False guaranty prohibited--Reliance on guaranty by another.

Section 39-18-32 - False or misleading advertising prohibited--Restrictions on liability of advertising media.

Section 39-18-33 - Sale of unrefrigerated biological products prohibited.

Section 39-18-34 - Exemption of veterinarians.

Section 39-18-34.1 - Relationship between veterinarian and client or patient as condition of dispensing certain drugs--What constitutes a valid relationship.

Section 39-18-35 - Enforcement of chapter--Rules and regulations--Notice and hearing on regulations.

Section 39-18-36 - Publication of production data and analysis results--Operations not disclosed.

Section 39-18-37 - Violation of chapter or rules and regulations as misdemeanor.

Section 39-18-38 - Investigations pertinent to enforcement.

Section 39-18-39 - Access of departmental personnel to premises.

Section 39-18-40 - Procurement and analysis of samples--Official analysis as sole guide for administrative determinations.

Section 39-18-41 - Refusal of inspection or sample prohibited.

Section 39-18-42 - Analysis result showing adulteration or misbranding forwarded to distributor and purchaser--Portion of sample furnished.

Section 39-18-43 - Unauthorized disclosure of information prohibited.

Section 39-18-44 - Withholding from sale of remedies not in compliance.

Section 39-18-45 - Tagging of adulterated or misbranded remedies--Disposal or removal from premises prohibited.

Section 39-18-46 - Petition for condemnation of adulterated or misbranded article--Removal of tag if found not adulterated or misbranded.

Section 39-18-47 - Destruction of article found adulterated or misbranded--Costs and expenses.

Section 39-18-48 - Bond to permit processing or relabeling of detained remedy--Expense of supervision--Return of bond on compliance.

Section 39-18-49 - Report of violations to prosecuting authorities.

Section 39-18-50 - Report for prosecution required for minor violations--Warning notice.

Section 39-18-51 - Prosecution of violations reported--Opportunity to present views before report for prosecution.

Section 39-18-52 - Severability of provisions.

Section 39-18-53 - Citation of chapter.