DermaRite recalls 4-oz skin protectant cream due to contamination risk from shared manufacturing facility with other products. Affected lots produced before August 2027. Consumers should contact DermaRite for details.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling a skin protectant cream because it was made at a facility that previously contaminated other products. This means the cream could contain harmful substances from the same manufacturing process.
The cream was manufactured at a facility that previously had contamination issues with other products. This means the cream could contain harmful substances from the same manufacturing process. However, the specific contamination risk is not described as causing serious injury.
People who own the 4-ounce skin cream with NDC 61924-208-04 produced before August 2027 are affected. Those with sensitive skin may be at slightly higher risk due to potential contamination.
Check for the product name '4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%', 113g (4 oz) per bottle, and NDC 61924-208-04. The lot was produced on or before August 2027.
Look for the NDC code 61924-208-04 and production date before August 2027 on the bottle.
The recall states there is a contamination risk from the manufacturing facility, but does not specify if the product is safe to use. Consumers should contact DermaRite for details.
The recall record does not mention a replacement or remedy for this product.
The recall record does not specify a remedy, so consumers should check with DermaRite directly for guidance.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0160-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0160-2026 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.
