Kenil Healthcare recalls Optim V Anti-Itch Cream due to manufacturing deviations. This cream contains Benzocaine 20% and Resorcinol 3% and may pose quality risks. Consumers should check product details and contact the manufacturer for guidance.
CGMP Deviations
Kenil Healthcare is recalling Optim V Anti-Itch Cream (Benzocaine 20% & Resorcinol 3%) because of manufacturing deviations. This recall affects products made in India with specific lot and expiration dates. The issue could impact product safety and quality, but no injuries have been reported.
The product was manufactured in India with a specific lot number and expiration date. Manufacturing deviations (CGMP) could affect the product's safety and quality, but the exact nature of the deviations is not detailed in the recall notice.
People who own or use Optim V Anti-Itch Cream with the specific lot number SP24A and expiration date 09/30/2026 are affected. Those using the product for analgesic purposes may be at risk due to manufacturing deviations.
Check for the lot number SP24A and expiration date 09/30/2026 on the tube. The product is distributed by Pharmadel LLC and made in India with NDC 55758-300-01 and UPC 8 59424 00420 6.
Look for the lot number SP24A and expiration date 09/30/2026 on the tube.
Optim V Anti-Itch Cream (Benzocaine 20% & Resorcinol 3%) with lot number SP24A and expiration date 09/30/2026.
The recall is due to CGMP deviations in manufacturing, which could affect product safety and quality.
Check for the lot number SP24A and expiration date 09/30/2026 on the tube. The product is distributed by Pharmadel LLC and made in India with NDC 55758-300-01 and UPC 8 59424 00420 6.
We’ve drafted a message you can send Kenil Healthcare to request your refund or repair — edit it as you like.
Subject: Recall D-0427-2025 — Kenil Healthcare Kenil Healthcare Hello, I own a Kenil Healthcare that is covered by recall D-0427-2025 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.
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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.
