DermaRite Industries recalls antifungal cream with 2% miconazole nitrate due to contamination at shared manufacturing facility. Products with NDC 61924-234-05 (5g packets) or NDC 61924-234-04 (106g tubes) sold by or for 08/2027 expiry date.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling antifungal cream products that were made at a facility where contamination occurred. This could pose a risk of exposure to harmful substances if the cream is used.
The cream was manufactured at a facility that previously had contamination issues. This means the product could contain harmful substances that might cause skin irritation or allergic reactions in some users.
People who own or use the recalled antifungal cream products with NDC codes 61924-234-05 or 61924-234-04. Those with sensitive skin or allergies may be at higher risk.
Check for the NDC codes 61924-234-05 (5g packets) or 61924-234-04 (106g tubes) on the product packaging. Products were sold with an expiry date of 08/2027.
Look for NDC codes 61924-234-05 or 61924-234-04 on the packaging to identify recalled items.
The recall indicates a potential contamination risk at the manufacturing facility, but the product may still be safe for most users. Consult a healthcare provider if you have sensitive skin or allergies.
The recall does not specify a remedy, so you should check with the manufacturer or a healthcare provider for guidance.
Check the product packaging for NDC codes 61924-234-05 (5g packets) or 61924-234-04 (106g tubes). Products were sold with an expiry date of 08/2027.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0162-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0162-2026 from DermaRite. 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.
