Cipla Diclofenac Sodium Topical Gel Recall
Diclofenac Sodium Topical Gel, 1%, NET WT 100 g (3.53 oz), Manufactured by: DPT Laboratories, Ltd., 307 E Josephine Street, San Antonio, TX
Updated December 22, 2025
Cipla's Diclofenac Sodium Topical Gel 1% (100 g) is being recalled because it failed pH specifications, which may affect the product's stability and effectiveness.
Is the Cipla USA, Inc. recalled? Yes. This product was recalled by FDA on December 22, 2025. Details below.
What is recalled
Diclofenac Sodium Topical Gel, 1%, NET WT 100 g (3.53 oz), NDC 76282-103-39, manufactured by DPT Laboratories, Ltd., 307 E Josephine Street, San Antonio, TX 78215, and distributed under the Cipla USA, Inc. brand.
Am I affected
You're affected if you own a tube or container of Diclofenac Sodium Topical Gel 1% with NDC 76282-103-39 manufactured by DPT Laboratories, Ltd.
What to do right now
Stop using this product. Contact Cipla USA, Inc. or the place where you purchased it for instructions on return or replacement.
The hazard
Failed PH Specifications
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0291-2026
- Classification
- Class III
- Recalled
- December 22, 2025
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