Glenmark Pharmaceuticals recalls 0.1% Mometasone Furoate lotion due to defective container. Rx-only product with specific lot numbers and expiration dates. Consumers should check their bottles for affected lots.
Defective Container
Glenmark Pharmaceuticals is recalling two sizes of 0.1% Mometasone Furoate topical lotion because the container may be defective. This recall affects prescription-only products with specific lot numbers and expiration dates that could pose a risk if the container fails.
The container may be defective, which could lead to the lotion leaking or spilling. This might cause the medication to be ineffective or cause skin irritation if the product comes into contact with the skin in an unintended way.
Prescription users of Glenmark's 0.1% Mometasone Furoate lotion who have the specific bottle sizes and lot numbers listed in the recall. People with asthma or skin conditions requiring this medication are most at risk if the container fails.
Check the bottle size: 30 ml or 60 ml. Look for the lot numbers listed in the recall (e.g., 05201358, 05210287, etc.) and expiration dates (e.g., 06/2022, 01/2023, etc.).
Identify the bottle size (30 ml or 60 ml) and lot number to see if it matches the recalled items.
The recall states the container may be defective, so it's not safe to use until the issue is resolved. The product is prescription-only and should be used only as directed by a healthcare provider.
Check the bottle for the specific lot numbers and expiration dates listed in the recall. If it matches, stop using it and contact your doctor or pharmacist for further instructions.
The recall does not mention a replacement or remedy. Consumers should contact their doctor or pharmacist for guidance on what to do with the recalled product.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-1173-2022 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-1173-2022 from Glenmark. 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.
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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.
