Sun Pharmaceutical Industries Inc: Fluocinonide, Usp, 0.05% Cream

Sun Pharmaceutical is recalling Fluocinonide 0.05% Cream (a prescription steroid cream) in 30-gram tubes nationwide because the product's thickness was found to be higher than acceptable standards during stability testing. The affected product has NDC number 51672-1386-2 and was manufactured by Taro Pharmaceuticals in Canada. This is a Class II recall, meaning the product could cause adverse health effects but is unlikely to cause serious harm.

Recalling firm
SUN PHARMACEUTICAL INDUSTRIES INC
Product
Fluocinonide, USP, 0.05% Cream, 30g tube, Rx only, Mfd by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1, Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532, NDC 51672-1386-2.
Reason
Failed Viscosity Specifications: Out of Specification results, above the specification limit, in viscosity, noted during stability testing.
Classification
Class II
Category
drug recall
Country
United States
Agency
U.S. Food and Drug Administration
Recall date
2026-03-25
Status
Ongoing
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
Nationwide in the USA.

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/772756ba-ddb1-46d5-968a-219caa86aa49