Insight Pharmaceuticals recalls Americaine benzocaine topical anesthetic spray (2 oz) due to benzene contamination. Affected products have NDC 63736-378-02 and were made in India with specific lot numbers.
Chemical Contamination: presence of benzene
Insight Pharmaceuticals is recalling Americaine benzocaine topical anesthetic spray because it contains benzene, a known chemical contaminant. This poses a risk of harm to users, especially those with sensitive skin or respiratory issues.
Benzene is a known chemical contaminant that can cause skin irritation and respiratory issues. In high concentrations, it may lead to more serious health effects, particularly for individuals with sensitive skin or respiratory conditions.
People who own or use the Americaine benzocaine spray (2 oz) with NDC 63736-378-02 are affected. Those with sensitive skin or respiratory conditions may be at higher risk due to potential inhalation or skin irritation.
Check for the NDC code 63736-378-02 on the product label. The spray was made in India with lot number 1A16420 and expires January 31, 2025.
Look for the NDC code 63736-378-02 and lot number 1A16420 on the spray can.
The recall states the product contains benzene, a known chemical contaminant that can cause skin irritation and respiratory issues, so it is not safe to use.
The recall does not specify a remedy, so you should check the product label for the NDC code and lot number to confirm if it is affected.
The product was made in India with lot number 1A16420 and expires January 31, 2025.
We’ve drafted a message you can send Insight Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0236-2024 — Insight Pharmaceuticals Insight Pharmaceuticals Hello, I own a Insight Pharmaceuticals that is covered by recall D-0236-2024 from Insight Pharmaceuticals. 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.
