(1) DEFINITIONS. In this section:
(a) “Administer” means the direct application of a nonprescription drug product or prescription drug, whether by injection, ingestion or other means, to the human body.
(b) “Drug” means any substance recognized as a drug in the official U.S. pharmacopoeia and national formulary or official homeopathic pharmacopoeia of the United States or any supplement to either of them.
(bg) “Drug product” means a specific drug or drugs in a specific dosage form and strength from a known source of manufacture.
(br) “Epinephrine delivery system” means a device that is approved by the federal food and drug administration, that contains a premeasured dose of epinephrine, and that is used to administer epinephrine into the human body to prevent or treat a life-threatening allergic reaction.
(c) “Health care professional” means a person licensed as an emergency medical services practitioner under s. 256.15, a person certified as an emergency medical responder under s. 256.15 (8) or any person licensed, certified, permitted or registered under chs. 441 or 446 to 449.
(d) “High degree of negligence” means criminal negligence, as defined in s. 939.25 (1).
(dm) “Nonprescription drug product” means any nonnarcotic drug product which may be sold without a prescription order and which is prepackaged for use by consumers and labeled in accordance with the requirements of state and federal law.
(dr) “Opioid antagonist” has the meaning given in s. 450.01 (13v).
(dt) “Opioid-related drug overdose” has the meaning given in s. 256.40 (1) (d).
(e) “Practitioner” means any physician, naturopathic doctor, dentist, optometrist, physician assistant, advanced practice registered nurse with prescribing authority, or podiatrist licensed in any state.