(1) A requirement that a health care provider who is authorized to prescribe drugs in this state label a drug dispensed by the health care provider with the information described in subsection (2) of this section does not apply to a drug approved by the United States Food and Drug Administration for the reversal of an opioid overdose if the drug is:
(a) In the form of a nasal spray; and
(b) Personally dispensed by a health care provider described in this subsection at the location of practice of the health care provider.
(2) The information described in subsection (1) of this section includes:
(a) The name of the patient;
(b) The name and address of the dispensing health care provider;
(c) The date of dispensing;
(d)(A) The name of the drug or, if the dispensed drug does not have a brand name, the generic name of the drug along with the name of the drug distributor or manufacturer;
(B) The drug’s quantity per unit, unless the drug is a compound; and
(C) The directions for the drug’s use stated in the prescription;
(e) Cautionary statements, if any, as required by law; and
(f) When applicable and as determined by the State Board of Pharmacy, an expiration date after which the patient should not use the drug.