Glenmark Pharmaceuticals recalls 15% Azelaic Acid Gel 50g for gritty texture complaints. Rx-only product with NDC 68462-626-52. Consumers should check batch numbers and contact for details.
CGMP Deviations: Market complaints received for gritty texture (grainy)
Glenmark Pharmaceuticals is recalling 15% azelaic acid gel (50g) due to reports of gritty texture. This issue may cause discomfort or irritation for users applying the product topically.
The gel has a gritty texture that can cause skin irritation or discomfort when applied. This is a quality issue from manufacturing, not a safety hazard.
People with prescriptions for this topical acne treatment. Those applying the gel to skin are most at risk of irritation.
Check the product label for 'Azelaic Acid Gel 15%, 5:0g' and NDC 68462-626-52. The batch number starts with 19252524 and expires May 2027.
Look for the NDC code 68462-626-52 and batch number starting with 19252524.
The product is safe for topical use but may cause irritation due to gritty texture. Consult your doctor if you experience discomfort.
Check the product label for the NDC code and batch number. Contact Glenmark Pharmaceuticals for further instructions.
No serious injury risk is reported. The issue is a texture complaint that may cause mild irritation.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0662-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0662-2025 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.
