Minnesota Statutes
Chapter 151 — Pharmacy Practice And Wholesale Distribution Act
Section 151.26 — Exceptions.

Subdivision 1. Generally. Nothing in this chapter shall subject a person duly licensed in this state to practice medicine, dentistry, or veterinary medicine, to inspection by the State Board of Pharmacy, nor prevent the person from administering drugs, medicines, chemicals, or poisons in the person's practice, nor prevent a duly licensed practitioner from furnishing to a patient properly packaged and labeled drugs, medicines, chemicals, or poisons as may be considered appropriate in the treatment of such patient; unless the person is engaged in the dispensing, sale, or distribution of drugs and the board provides reasonable notice of an inspection.
Except for the provisions of section 151.37, nothing in this chapter applies to or interferes with the dispensing, in its original package and at no charge to the patient, of a legend drug that was packaged by a manufacturer and provided to the dispenser for dispensing as a professional sample. Samples of a controlled substance shall only be dispensed when one of the approved indications for the controlled substance is a seizure disorder and when the sample is prepared and distributed pursuant to Code of Federal Regulations, title 21, part 203, subpart D.
Nothing in this chapter shall prevent the sale of drugs, medicines, chemicals, or poisons at wholesale to licensed physicians, dentists and veterinarians for use in their practice, nor to hospitals for use therein.
Nothing in this chapter shall prevent the sale of drugs, chemicals, or poisons either at wholesale or retail for use for commercial purposes, or in the arts, nor interfere with the sale of insecticides, as defined in Minnesota Statutes 1974, section 24.069, and nothing in this chapter shall prevent the sale of common household preparations and other drugs, chemicals, and poisons sold exclusively for use for nonmedicinal purposes; provided that this exception does not apply to any compound, substance, or derivative that is not approved for human consumption by the United States Food and Drug Administration or specifically permitted for human consumption under Minnesota law, and, when introduced into the body, induces an effect similar to that of a Schedule I or Schedule II controlled substance listed in section 152.02, subdivisions 2 and 3, or Minnesota Rules, parts 6800.4210 and 6800.4220, regardless of whether the substance is marketed for the purpose of human consumption.
Nothing in this chapter shall apply to or interfere with the vending or retailing of any nonprescription medicine or drug not otherwise prohibited by statute that is prepackaged, fully prepared by the manufacturer or producer for use by the consumer, and labeled in accordance with the requirements of the state or federal Food and Drug Act; nor to the manufacture, wholesaling, vending, or retailing of flavoring extracts, toilet articles, cosmetics, perfumes, spices, and other commonly used household articles of a chemical nature, for use for nonmedicinal purposes; provided that this exception does not apply to any compound, substance, or derivative that is not approved for human consumption by the United States Food and Drug Administration or specifically permitted for human consumption under Minnesota law, and, when introduced into the body, induces an effect similar to that of a Schedule I or Schedule II controlled substance listed in section 152.02, subdivisions 2 and 3, or Minnesota Rules, parts 6800.4210 and 6800.4220, regardless of whether the substance is marketed for the purpose of human consumption. Nothing in this chapter shall prevent the sale of drugs or medicines by licensed pharmacists at a discount to persons over 65 years of age.
Subd. 2. [Repealed, 1973 c 639 s 11]
(5808-27) 1937 c 354 s 27; 1953 c 76 s 5; 1969 c 627 s 1; 1971 c 192 s 1; 1973 c 639 s 8; 1Sp1981 c 4 art 1 s 82; 1986 c 444; 1988 c 550 s 16; 2014 c 285 s 4; 2014 c 291 art 5 s 11

Structure Minnesota Statutes

Minnesota Statutes

Chapters 144 - 159 — Health

Chapter 151 — Pharmacy Practice And Wholesale Distribution Act

Section 151.01 — Definitions.

Section 151.02 — State Board Of Pharmacy.

Section 151.03 — Membership.

Section 151.04 — Recommended Names.

Section 151.05 — Election Of Officers.

Section 151.06 — Powers And Duties.

Section 151.061 — Unfair Price Discrimination.

Section 151.065 — Fee Amounts.

Section 151.066 — Opiate Product Registration Fee.

Section 151.07 — Meetings; Examination Fee.

Section 151.071 — Disciplinary Action.

Section 151.072 — Reporting Obligations.

Section 151.073 — Immunity.

Section 151.074 — Licensee Or Registrant Cooperation.

Section 151.075 — Disciplinary Record On Judicial Review.

Section 151.095 — Inactive Status License.

Section 151.10 — Qualifications Of Applicants.

Section 151.101 — Internship.

Section 151.102 — Pharmacy Technician.

Section 151.12 — Reciprocity; Licensure.

Section 151.13 — Renewal Fee; Continuing Education.

Section 151.14 — Reinstatements.

Section 151.15 — Compounding Drugs Unlawful Under Certain Conditions.

Section 151.16 — Violation A Gross Misdemeanor.

Section 151.17 — Unlawful Use Of "pharmacist."

Section 151.18 — Unlawful To Use Misleading Name.

Section 151.19 — Registration; Fees.

Section 151.191 — Licensing Medical Gas Facilities; Fees; Prohibitions.

Section 151.21 — Substitution.

Section 151.211 — Records Of Prescriptions.

Section 151.212 — Label Of Prescription Drug Containers.

Section 151.213 — Copies Of Prescriptions.

Section 151.214 — Payment Disclosure.

Section 151.215 — Certification.

Section 151.22 — Liability For Quality Of Drugs.

Section 151.23 — Poisons Must Be Labeled.

Section 151.24 — Sale Of Poisons Must Be Recorded.

Section 151.252 — Licensing Of Drug Manufacturers; Fees; Prohibitions.

Section 151.253 — Compounding.

Section 151.26 — Exceptions.

Section 151.27 — Expenses.

Section 151.29 — Violation A Misdemeanor.

Section 151.30 — County Attorney To Prosecute.

Section 151.301 — Reports To Commissioner Of Health.

Section 151.302 — Immunity.

Section 151.32 — Citation.

Section 151.33 — Careless Distribution Of Drugs.

Section 151.335 — Delivery Through Common Carrier; Compliance With Temperature Requirements.

Section 151.34 — Prohibited Acts.

Section 151.35 — Drugs, Adulteration.

Section 151.36 — Drugs, Misbranding.

Section 151.361 — Manufacturer Disclosure.

Section 151.37 — Legend Drugs; Who May Prescribe, Possess.

Section 151.375 — Investigational Drug Use.

Section 151.38 — Embargoes.

Section 151.39 — Distressed Drugs.

Section 151.40 — Possession And Sale Of Hypodermic Syringes And Needles.

Section 151.415 — Long-term Care Resident Access To Pharmaceuticals Act.

Section 151.43 — Scope.

Section 151.441 — Definitions.

Section 151.46 — Prohibited Drug Purchases Or Receipt.

Section 151.461 — Gifts To Practitioners Prohibited.

Section 151.47 — Wholesale Drug Distributor Licensing Requirements.

Section 151.471 — Third-party Logistics Provider Requirements.

Section 151.555 — Prescription Drug Repository Program.

Section 151.56 — County Return Of Unused Drugs Or Medical Devices.

Section 151.58 — Automated Drug Distribution Systems.

Section 151.72 — Sale Of Certain Cannabinoid Products.

Section 151.74 — Insulin Safety Net Program.