DermaRite recalls Lantiseptic Dry Skin Therapy (30% lanolin) due to contamination at shared manufacturing facility. Affected lots expire 08/2027. Consumers should check NDC codes and contact DermaRite for details.
CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
DermaRite is recalling Lantiseptic Dry Skin Therapy products that may have been contaminated during manufacturing. This recall is due to a contamination risk at a shared facility, which could pose health hazards if the product is used.
The products were manufactured at a facility that previously had contamination issues with other products. This means the lanolin-based skin therapy could contain harmful substances that might cause skin irritation or infection if used.
People who own or use Lantiseptic Dry Skin Therapy products with NDC codes 61924-504-05, 61924-504-04, or 61924-710-14. Those with sensitive skin or open wounds may be at higher risk due to potential contamination.
Check the product label for NDC codes 61924-504-05 (5g), 61924-504-04 (4oz), or 61924-710-14 (14oz). The products expire by August 2027.
Look for NDC codes 61924-504-05, 61924-504-04, or 61924-710-14 on the packaging.
The recall states there is a contamination risk at the manufacturing facility, so it is not recommended to use these products until the recall is resolved.
Check the product label for NDC codes 61924-504-05, 61924-504-04, or 61924-710-14. Products with these codes are affected.
The recall does not specify a remedy, so contact DermaRite directly for guidance on next steps.
We’ve drafted a message you can send DermaRite to request your refund or repair — edit it as you like.
Subject: Recall D-0169-2026 — DermaRite DermaRite Hello, I own a DermaRite that is covered by recall D-0169-2026 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.
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.
