Ciclopirox Gel 0.77% recall
Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm Tube, NDC 68462-0455-47; c)…
Why was Ciclopirox Gel 0.77% recalled?
Defective Container: Firm received complaints of broken tube at the seal.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #s: a) 19242028, Exp. 04/30/2026; b) 19242028, Exp. 04/30/2026; c) 19242028, Exp. 04/30/2026
- Product
- Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for Use in Eyes, Rx Only, a) 30 gm Tube, NDC 68462-0455-35; b) 45 gm Tube, NDC 68462-0455-47; c)…
- Recalling firm
- Glenmark Pharmaceuticals Inc., USA
- Quantity
- 11,568 tubes
- Distribution
- Nationwide in the US.
- Recall date
- October 9, 2024
- Classification
- Class III
- Status
- Ongoing
- Agency
- FDA (drug)