Sun Pharmaceutical recalls 0.05% Fluocinonide cream due to failed viscosity tests. This may affect stability and safety. Check your product details to see if it's affected.
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
Sun Pharmaceutical 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, potentially affecting its safety and effectiveness.
The cream failed viscosity tests, meaning it may not stay stable over time. This could lead to inconsistent strength or separation, but it's unlikely to cause serious harm in normal use.
People with prescriptions for this cream, especially those using it for skin conditions. Those with sensitive skin or using it long-term may be at slightly higher risk.
Check for the 60g tube labeled 'Fluocinonide, USP, 0.05% Cream, Rx only'. The product was manufactured by Taro Pharmaceuticals Inc. in Brampton, Ontario, Canada, with lot number AD76250 and expiration date 6/30/2026.
Look for the 60g tube with the product code NDC 51672-1386-3 and lot number AD76250.
The recall is due to failed viscosity tests, but the product is still safe for use as long as it's within the expiration date and stored properly.
Check for the lot number AD76250 and expiration date 6/30/2026 on the tube. The product was made by Taro Pharmaceuticals Inc. in Brampton, Ontario, Canada.
The recall doesn't require immediate action, but you should check the product details to confirm if it's affected. If it is, contact your doctor or pharmacist.
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-0477-2026 — Sun Pharmaceutical Industries Sun Pharmaceutical Industries Hello, I own a Sun Pharmaceutical Industries that is covered by recall D-0477-2026 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.
