Sun Pharmaceutical Industries recalls 0.05% Fluocinonide cream due to failed viscosity testing. This may affect product stability and safety. Consumers should contact the manufacturer for details.
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
Sun Pharmaceutical Industries is recalling 0.05% Fluocinonide cream tubes that failed viscosity testing during stability checks. This could mean the product doesn't stay stable as intended, but the recall doesn't specify immediate safety risks.
The cream failed viscosity tests, meaning it may not stay stable over time. This could lead to inconsistent strength or separation, but the recall doesn't mention immediate safety risks like injury or serious harm.
People with prescriptions for this cream, especially those using it for skin conditions. Those who have the specific tube size and lot number are most at risk.
Check for the 15g tube labeled 'Fluocinonide, USP, 0.05% Cream', manufactured by Taro Pharmaceuticals Inc. in Brampton, Ontario, Canada, with lot number AD76252 and expiration date 6/30/2026.
Look for the tube size, lot number, and expiration date on the product label.
The recall states the product failed viscosity testing, but it does not mention immediate safety risks like injury or serious harm.
Check for the 15g tube labeled 'Fluocinonide, USP, 0.05% Cream', manufactured by Taro Pharmaceuticals Inc. in Brampton, Ontario, Canada, with lot number AD76252 and expiration date 6/30/2026.
The recall does not specify a remedy, so contact Sun Pharmaceutical Industries for further instructions.
We’ve drafted a message you can send Sun Pharmaceutical Industries to request your refund or repair — edit it as you like.
Subject: Recall D-0475-2026 — Sun Pharmaceutical Industries Sun Pharmaceutical Industries Hello, I own a Sun Pharmaceutical Industries that is covered by recall D-0475-2026 from Sun Pharmaceutical Industries. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
