1. (a) The label of each drug or device shall be typed or machine-printed and shall include the following information:

   1. (1) The name, address, and telephone number of the pharmacy dispensing the prescription;
   2. (2) the name of the prescriber;
   3. (3) the full name of the patient;
   4. (4) the identification number assigned to the prescription by the dispensing pharmacy;
   5. (5) the date the prescription was filled or refilled;
   6. (6) adequate directions for use of the drug or device;
   7. (7) the beyond-use date of the drug or device dispensed;
   8. (8) the brand name or corresponding generic name of the drug or device;
   9. (9) the name of the manufacturer or distributor of the drug or device, or an easily identified abbreviation of the manufacturer's or distributor's name;
   10. (10) the strength of the drug;
   11. (11) the contents in terms of weight, measure, or numerical count; and
   12. (12) necessary auxiliary labels and storage instructions, if needed.
2. (b) A pharmacy shall be permitted to label or relabel only those drugs or devices originally dispensed from the providing pharmacy.

(Authorized by K.S.A. 65-1630; implementing K.S.A. 65-1626a; effective, E-77-39, July 22, 1976; effective Feb. 15, 1977; amended May 1, 1978; amended May 1, 1980; amended May 1, 1988; amended June 6, 1994; amended March 20, 1995; amended April 28, 2000; amended Oct. 23, 2009.)