Dabur India Limited recalls Med Pride 1% Clotrimazole Antifungal Cream due to FDA inspection findings of manufacturing deviations. Affected lots from 001 to 013, manufactured in India for US distribution.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India Limited is recalling Med Pride 1% Clotrimazole Antifungal Cream because FDA inspections found manufacturing deviations. This affects specific lots produced in India for US distribution. Consumers should check their product labels for the lot numbers listed.
The FDA identified manufacturing deviations during an inspection. These deviations could mean the product does not meet safety and quality standards, potentially affecting its effectiveness and safety for use on skin.
People who own or use the recalled Med Pride 1% Clotrimazole Antifungal Cream with lot numbers 001 through 013 are affected. Those using the product for skin conditions may be at risk if the cream does not meet quality standards.
Check the product label for the lot number, which should be between 001 and 013. The product is manufactured in India for US distribution with a net weight of 1 ounce (28.3g).
Look for the lot number on the label, which should be between 001 and 013 for affected products.
The FDA found manufacturing deviations during an inspection, which could affect the product's safety and quality.
Lot numbers 001 through 013 are affected.
Check the product label for the lot number, which should be between 001 and 013. The product is manufactured in India for US distribution with a net weight of 1 ounce (28.3g).
We’ve drafted a message you can send Dabur to request your refund or repair — edit it as you like.
Subject: Recall D-0638-2026 — Dabur Dabur Hello, I own a Dabur that is covered by recall D-0638-2026 from Dabur. 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.
