Flurandrenolide Ointment
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This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition
Issued and maintained by the United States Pharmacopeial Convention (USP)
Flurandrenolide Ointment contains not less than 90.0 percent and not more than 110.0 percent of the labeled amount of flurandrenolide (C24H33FO6 ).
Packaging and storage—Preserve in tight containers, protected from light.
USP Reference standards 〈11〉—
USP Flurandrenolide RS
Identication—It meets the requirements for Thin-layer chromatographic identification test under Flurandrenolide Cream. Microbial enumeration tests 〈61〉 and Tests for specified microorganisms 〈62〉—It meets the requirements of the tests for absence of Staphylococcus aureus and Pseudomonas aeruginosa.
Minimum fill 〈755〉: meets the requirements.
Assay—Proceed as directed in the Assay under Flurandrenolide Cream, using Ointment in place of Cream.
