Nystatin and Triamcinolone Acetonide Cream

This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition

Issued and maintained by the United States Pharmacopeial Convention (USP)

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Nystatin and Triamcinolone Acetonide Cream contains not less than 90.0 percent and not more than 140.0 percent of the labeled amount of USP Nystatin Units and not less than 90.0 percent and not more than 110.0 percent of the labeled amount of triamcinolone acetonide (C₂₄H₃₁FO₆).

Packaging and storage-Preserve in tight containers.

USP REFERENCE STANDARDS (11)

USP Nystatin RS

USP Triamcinolone Acetonide RS

Identification-Place 2 g of Cream in a conical flask, add 5.0 mL of chloroform, and shake for 10 minutes. Add 15 mL of alcohol, and shake for an additional 10 minutes. Filter the solution into a centrifuge tube, and evaporate the filtrate to dryness. Dissolve the residue in alcohol to obtain a solution containing about 250 µg of triamcinolone acetonide per ml. Proceed as directed in the Identification test under Triamcinolone Acetonide Cream, beginning with "Apply 10 µl of this solution": the specified result is observed.

MINIMUM FILL (755): meets the requirements.

Assay for nystatin-Proceed as directed for nystatin under Antibiotics-Microbial Assays (81), blending a suitable, accurately weighed portion of Cream in a high-speed blender for 3 to 5 minutes with a sufficient, accurately measured volume of dimethylformamide to give a convenient concentration. Dilute an accurately measured volume of the solution so obtained quantitatively with dimethylformamide to obtain a stock solution containing about 400 USP Nystatin Units per mL. Dilute an accurately measured volume of this stock solution quantitatively with Buffer B.6 to obtain a Test Dilution having a concentration of nystatin assumed to be equal to the median dose level of the Standard.

Assay for triamcinolone acetonide-Proceed with Cream as directed in the Assay under Triamcinolone Acetonide Cream.