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HF3832 • 2026

Definition of compounding of a drug amended to exempt the use of a flavoring agent.

Definition of compounding of a drug amended to exempt the use of a flavoring agent.

Passed Legislature

This bill passed both chambers and reached final enrollment, even if later executive action is not shown here.

Sponsor
Zeleznikar, Carroll
Last action
2026-03-12
Official status
Committee report, to adopt
Effective date
Not listed

Plain English Breakdown

The plain English breakdown is still being put together. The official documents below are already here.

Bill History

  1. 2026-03-12 House

    Committee report, to adopt

  2. 2026-03-02 House

    Introduction and first reading, referred to Health Finance and Policy

Official Summary Text

Definition of compounding of a drug amended to exempt the use of a flavoring agent.

Current Bill Text

Read the full stored bill text
A bill for an act

relating to health; amending the definition of compounding of a drug to exempt

the use of a flavoring agent; amending Minnesota Statutes 2024, section 151.01,

subdivision 35, by adding a subdivision.

BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF MINNESOTA:

Section 1.

Minnesota Statutes 2024, section 151.01, subdivision 35, is amended to read:

Subd. 35.

Compounding.

"Compounding" means preparing, mixing, assembling,

packaging, and labeling a drug for an identified individual patient as a result of a practitioner's

prescription drug order. Compounding also includes anticipatory compounding, as defined

in this section, and the preparation of drugs in which all bulk drug substances and components

are nonprescription substances. Compounding does not include mixing or reconstituting a

drug according to the product's labeling or to the manufacturer's directions, provided that

such labeling has been approved by the United States Food and Drug Administration (FDA)

or the manufacturer is licensed under section
151.252
. Compounding does not include the

preparation of a drug for the purpose of, or incident to, research, teaching, or chemical

analysis, provided that the drug is not prepared for dispensing or administration to patients.

All compounding, regardless of the type of product, must be done pursuant to a prescription

drug order unless otherwise permitted in this chapter or by the rules of the board.

Compounding does not include a minor deviation from such directions with regard to

radioactivity, volume, or stability, which is made by or under the supervision of a licensed

nuclear pharmacist or a physician, and which is necessary in order to accommodate

circumstances not contemplated in the manufacturer's instructions, such as the rate of

radioactive decay or geographical distance from the patient.
new text begin
Compounding does not include

the use of a flavoring agent to flavor a drug.
new text end

Sec. 2.

Minnesota Statutes 2024, section 151.01, is amended by adding a subdivision to

read:

new text begin

Subd. 44.

new text end

new text begin

Flavoring agent.

new text end

new text begin

"Flavoring agent" means a therapeutically inert, nonallergenic

substance consisting of inactive ingredients that is added to a drug to improve the drug's

taste and palatability.

new text end