One or more labels containing the following information shall be affixed to every container in which a prescription drug order is dispensed:

1. (1) name, address, and phone number of the dispensing pharmacy;
2. (2) unique identification number of the prescription drug order;
3. (3) date the prescription drug order is dispensed;
4. (4) initials, which may be handwritten, of the dispensing pharmacist or pharmacist intern;
5. (5) name of the prescribing practitioner;
6. (6) name of the patient or, if the drug was prescribed for an animal, the species of animal and the name of the owner;
7. (7) directions for use;
8. (8) quantity dispensed;
9. (9) appropriate ancillary instructions or cautions;
10. (10) if the prescription drug order is for a schedule II-V controlled substance, the statement, "Caution: Federal law prohibits the transfer of this drug to any person other than the patient for whom it was prescribed";
11. (11) the name and strength of the actual drug product dispensed, unless otherwise directed by the prescribing practitioner;
12. (12) the accepted generic drug name and strength of the drug dispense; if the drug product dispensed has multiple ingredients, the pharmacist shall provide this information in writing to the patient or the patient's agent.

(Eff. 1/16/98, Register 145; am 1/14/2004, Register 169; am 2/15/2006, Register 177; am 4/3/2020, Register 234)

Authority: AS 08.80.005, AS 08.80.030, AS 08.80.295, AS 08.80.480