4729-31-03 Labeling.

When prepared in a fluid therapy pharmacy, no compounded parenteral product prescription may be dispensed unless a label is affixed to the container in which such drug is dispensed and such label includes:

(A) The telephone number of the pharmacy, and the name and address of the pharmacy as it appears on the terminal distributor of dangerous drugs license;

(B) The full name of the patient for whom the drug is prescribed;

(C) The full name of the prescriber;

(D) Directions for use of the drug which must include route of administration;

(E) The date of dispensing;

(F) Any cautions which may be required by federal or state law;

(G) The name and amount of the drug(s) added;

(H) The name and volume of the parenteral solution;

(I) The quantity of drug dispensed, if appropriate;

(J) Beyond use date;

(K) Storage conditions.

Effective: 01/01/2011
R.C. 119.032 review dates: 12/01/2013
Promulgated Under: 119.03
Statutory Authority: 3715.69, 3719.28, 4729.26
Rule Amplifies: 3715.64, 3719.08
Prior Effective Dates: 3/1/99, 1/1/04, 1/1/09