Dabur India recalls Lucky Super Soft antifungal athlete's foot cream due to FDA inspection findings of manufacturing process deviations. Affected lots from specific manufacturers and dates.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India is recalling Lucky Super Soft athlete's foot cream with clotrimazole 1% due to FDA inspection finding manufacturing process deviations. This could affect product safety and quality.
The FDA found manufacturing process deviations during an inspection. This means the product may not meet safety and quality standards, though the exact risk isn't specified in the recall notice.
People who purchased the specific lot numbers (0001, 0002) of the 1.5 oz tubes from Dabur India Limited, manufactured for Delta Brands Inc. in New York.
Check for the product name 'Lucky Super Soft', clotrimazole 1% cream, 1.5 oz (42.5g) tubes with lot numbers 0001 or 0002. The product was manufactured for Delta Brands Inc. in Tarrytown, NY.
Look for the product name, lot numbers 0001 or 0002, and the 1.5 oz tube size on the packaging.
The FDA found manufacturing process deviations during an inspection, which could affect product safety and quality.
The recall notice doesn't specify a remedy, so check the product details and contact Dabur India Limited for further instructions.
Yes, lot numbers 0001 and 0002 are affected.
We’ve drafted a message you can send Dabur India to request your refund or repair — edit it as you like.
Subject: Recall D-0629-2026 — Dabur India Dabur India Hello, I own a Dabur India that is covered by recall D-0629-2026 from Dabur India. 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.
