Dabur India Limited recalls Lucky Super Soft antibiotic ointment due to FDA inspection findings. Affected lots from 2023-2024 may pose quality risks. Consumers should check product labels for lot numbers.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India Limited is recalling Lucky Super Soft and First Aid Triple Antibiotic Ointment products due to FDA inspection findings of manufacturing quality issues. This recall affects consumers who may have used these ointments, though no injuries have been reported.
The FDA identified manufacturing quality deviations during their inspection. These deficiencies could potentially affect the product's safety and effectiveness, though the specific risks are not detailed in the recall notice.
People who own or use Lucky Super Soft or First Aid Triple Antibiotic Ointment products from Dabur India Limited. Those who used the ointment during the specified manufacturing period are most at risk.
Check the product label for the brand name 'Dabur', product name 'Lucky Super Soft' or 'First Aid Triple Antibiotic Ointment', and lot numbers 0002 or 0003. The product was manufactured in India and sold in the US with a net weight of 0.5 oz (14g).
Look for the brand name 'Dabur', product name 'Lucky Super Soft' or 'First Aid Triple Antibiotic Ointment', and lot numbers 0002 or 0003.
The FDA found manufacturing quality deviations during their inspection of the product.
Check the product label for lot numbers 0002 or 0003. If you have these lots, contact Dabur India Limited for further instructions.
The recall notice states there were manufacturing quality issues, but no specific injuries have been reported.
We’ve drafted a message you can send Dabur to request your refund or repair — edit it as you like.
Subject: Recall D-0630-2026 — Dabur Dabur Hello, I own a Dabur that is covered by recall D-0630-2026 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.
