Sun Pharmaceutical Industries, Inc. recalls KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g), 15 g bottle, Physician Sampl
Recalled November 30, 2016 · FDA recall D-0148-2017 · Sun Pharmaceutical Industries
Hazard
Failed Stability Specifications: Low Out of Specification results for alcohol content. · FDA Class III
Units
326,103 bottles
Sold at
NJ and further distributed Nationwide in the USA.
Description
Failed Stability Specifications: Low Out of Specification results for alcohol content.
Product
KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol, USP, (0.147 mg/g), 15 g bottle, Physician Sample: Not For Sale, Rx only, RANBAXY, Jacksonville, FL 32257, UPC 3 10631 09335 8.
Manufacturer(s)
Sun Pharmaceutical Industries, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →