Dabur India Limited recalls Cura Hongos, Crema Antifungica, and Clotrimazole : FDA found manufacturing defects during inspection. Stop using immediately if you have these products.
CGMP Deviations; deficiencies observed during FDA inspection
Dabur India Limited is recalling Cura Hongos, Crema Antifungica, and Clotrimazole 1% tubes due to FDA inspection findings of manufacturing deviations. This recall is important because the products may contain unsafe levels of ingredients that could cause harm.
The FDA identified manufacturing deviations during an inspection, which could mean the products contain unsafe levels of ingredients. This might lead to adverse health effects if the products are used as intended.
People who own or use the recalled Cura Hongos, Crema Antifungica, or Clotrimazole 1% tubes made in India with the specified UPC and lot number are affected. Those using these products for fungal infections are at higher risk.
Check for the product names Cura Hongos, Crema Antifungica, or Clotrimazole 1% in 2oz (57g) tubes. Look for the UPC 8 52924 00683 1 and lot number 0003 on the packaging.
Discard any recalled Cura Hongos, Crema Antifungica, or Clotrimazole 1% tubes if you have them.
The FDA found manufacturing deviations during an inspection, which could mean the products contain unsafe levels of ingredients.
Discard the product immediately and contact Dabur India Limited for a replacement if needed.
Yes, the lot number 0003 is associated with this recall.
We’ve drafted a message you can send Dabur to request your refund or repair — edit it as you like.
Subject: Recall D-0634-2026 — Dabur Dabur Hello, I own a Dabur that is covered by recall D-0634-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
