Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol Recalled by Sun Pharmaceutical Industries, Inc. Due to Failed Stability Specifications: Low Out of Specification results...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Sun Pharmaceutical Industries, Inc. directly.
Affected Products
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.
Quantity: 326,103 bottles
Why Was This Recalled?
Failed Stability Specifications: Low Out of Specification results for alcohol content.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sun Pharmaceutical Industries, Inc.
Sun Pharmaceutical Industries, Inc. has 40 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report