DermaRite Industries recalls Renew PeriProtect zinc oxide cream due to contamination at manufacturing facility. Products with NDC 61924-435-04 and expiry 08/2027 may pose contamination risk.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite Industries is recalling Renew PeriProtect zinc oxide cream because it was made at a facility that contaminated other products. This could mean the cream might have harmful substances that could cause health issues if used.
The cream was manufactured at a facility that previously had contamination issues with other products. This means the cream might contain harmful substances that could cause health problems if used, but the specific risk is not severe enough to cause serious injury.
People who own or use Renew PeriProtect zinc oxide cream with NDC 61924-435-04 and expiry date 08/2027 are affected. Those with sensitive skin or using the product for extended periods may be at slightly higher risk.
Check for the NDC code 61924-435-04 on the product label. Products with expiry dates up to 08/2027 are included in this recall.
Look for the NDC code 61924-435-04 and expiry date up to 08/2027 on the product label.
The recall states there is a risk of contamination at the manufacturing facility, but the specific health risk is not severe enough to cause serious injury. The product may still be safe for most users.
The recall does not specify a remedy, so no action is required beyond checking the product label for the NDC code and expiry date.
Check for the NDC code 61924-435-04 and expiry date up to 08/2027 on the product label.
We’ve drafted a message you can send DermaR: Renew PeriProtect to request your refund or repair — edit it as you like.
Subject: Recall D-0174-2026 — DermaR: Renew PeriProtect DermaR: Renew PeriProtect Hello, I own a DermaR: Renew PeriProtect that is covered by recall D-0174-2026 from DermaR: Renew PeriProtect. 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.
