Kenil Healthcare is recalling Curahongos 1% Clotrimazole topical lotion due to CGMP deviations. The product may not meet safety standards. Consumers should check the lot number on the label.
CGMP Deviations
Kenil Healthcare is recalling a specific antifungal lotion product because of manufacturing deviations that could affect safety. This recall affects consumers who have the product with the described lot number and expiration date.
The product was made under CGMP (Current Good Manufacturing Practices) deviations, which are regulatory standards for product safety. These deviations could mean the lotion does not meet the required safety standards, potentially leading to health risks if used improperly.
Anyone who owns or uses the recalled Curahongos antifungal lotion with the lot number SP31A and expiration date 09/30/2026 is affected. People using this product for fungal infections may be at risk if the manufacturing deviations impact safety.
Check the label for the lot number SP31A and expiration date 09/30/2026. The product is a 0.76 fl oz (22.5 mL) bottle made in India with NDC 55758-34-01.
Look for the lot number SP31A and expiration date 09/30/2026 on the bottle.
The recall states there were CGMP deviations, which could affect safety, but the official notice does not specify if the product is safe to use.
Check the label for the lot number SP31A and expiration date 09/30/2026 on the 0.76 fl oz (22.5 mL) bottle.
The recall does not specify a remedy, so the official notice does not say what to do next.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0422-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0422-2025 from Kenil Healthcare. 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.
