Dermoplast recalls first aid antibacterial spray with low assay of active ingredients. This may not be as effective as intended. Consumers should check product details and contact manufacturer for guidance.
Subpotent Drug: Low assay observed in one of the two active ingredients during stability testing.
Dermoplast is recalling its First Aid Antibacterial Spray due to low levels of active ingredients observed during testing. This could mean the product isn't as effective as it should be, but it's not an immediate safety risk.
The spray contains benzethonium chloride and benzocaine. During stability testing, the product showed lower levels of these active ingredients than expected. This means the spray might not work as well for treating minor wounds.
People who own or use Dermoplast First Aid Antibacterial Spray (2.75 oz) with NDC# 16864-670-01 and Lot # 22336A are affected. Those using the product for minor cuts or scrapes may be at slightly higher risk if the product isn't effective.
Check for the product name 'Dermoplast FIRST AID ANTIBACTERIAL SPRAY' with a 2.75 oz (78 g) size. Look for NDC# 16864-670-01 and Lot # 22336A on the label.
Look for NDC# 16864-670-01 and Lot # 22336A on the label to confirm if the product is recalled.
No, the recall is due to low levels of active ingredients, not an immediate safety risk. The product is still safe for minor use but may not work as effectively.
Check the product label for NDC# 16864-670-01 and Lot # 22336A. If it matches, contact Dermoplast for guidance.
The recall does not provide a fix. Consumers should check the product details and contact the manufacturer if needed.
We’ve drafted a message you can send Dermoplast to request your refund or repair — edit it as you like.
Subject: Recall D-0329-2023 — Dermoplast Dermoplast Hello, I own a Dermoplast that is covered by recall D-0329-2023 from Dermoplast. 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.
