Nevada Administrative Code
Chapter 639 - Pharmacists and Pharmacy
COMPOUNDING AND DISPENSING DRUG PRODUCTS
Standards for Compounding and Dispensing Nonsterile Products
Section 639.6703 - Labeling

Universal Citation: NV Admin Code 639.6703

Current through December 12, 2024

1. Each pharmacist engaged in the practice of compounding nonsterile compounded drug products shall label each nonsterile compounded drug product, including, without limitation, any amount of the nonsterile compounded drug product that is in excess of the amount required by the prescription or chart order and any nonsterile compounded drug product that is compounded in bulk quantities. The label must include, without limitation:

(a) The name of the final compounded drug product or the name of each active ingredient present in the nonsterile compounded drug product and, as appropriate, the concentration of each active ingredient in the final compounded drug product;

(b) The internal control number assigned to the compounded drug product by the pharmacist; and

(c) The beyond-use date of the compounded drug product.

2. Each pharmacist engaged in the practice of compounding nonsterile compounded drug products shall ensure that each nonsterile compounded drug product, including, without limitation, any amount of the nonsterile compounded drug product that is in excess of the amount required by the prescription or chart order, and any nonsterile compounded drug product that is compounded in bulk quantities is stored in the pharmacy in a manner that:

(a) Maintains the efficacy of the nonsterile compounded drug product; and

(b) Ensures that the nonsterile compounded drug product remains free from contamination.

Added to NAC by Bd. of Pharmacy by R035-06, eff. 9-18-2008; A by R053-24A, eff. 10/23/2024

NRS 639.070

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