Clobetasol Propionate Foam recall
Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (NDC 68462-625-94), Rx Only, Manufactured…
Why was Clobetasol Propionate Foam recalled?
Defective delivery system; product is not foaming or is coming out as liquid.
What should I do if I have this product?
Review the official FDA enforcement record for current 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 14190067, exp Jul-2021
- Product
- Clobetasol Propionate Foam (Emulsion Formulation), 0.05% a) 50 g pack (NDC 68462-625-27) and b) 100 g pack (NDC 68462-625-94), Rx Only, Manufactured…
- Recalling firm
- Glenmark Pharmaceuticals Inc., USA
- Quantity
- a) 480 packs; b) 240 packs
- Distribution
- Nationwide
- Recall date
- December 18, 2019
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)