Curacaine
Product Images NDC 51350-011

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Curacaine (NDC 51350-011). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Transdermal Corp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Curacaine Box_back (Curacaine Box Back)

Drug Facts panel for CURACAINE with 4% Lidocaine as the active ingredient, a topical analgesic. The panel includes uses for temporary relief of pain and itching from insect bites, sunburn, minor cuts, and minor skin irritations, warnings for external use only, directions for application, and storage instructions. It advises keeping out of reach of children and consulting a physician if symptoms persist or worsen.*

FDA Label Image

Curacaine Box_front (Curacaine Box Front)

CURACAINE topical analgesic packaging label by Transdermal Corp. The label highlights the product as a rapid acting, maximum strength topical analgesic containing 4% lidocaine. It promotes relief of itching and pain associated with conditions such as insect bites, sunburn, minor cuts, burns, and minor skin irritations. The net weight is 1 fl oz (30 ml).*

FDA Label Image

Curacaine Tube (Curacaine Tube)

CURACAINE Rapid Acting Topical Analgesic label. Yellow and dark blue carton with text indicating scientific advancement for itching and pain relief. Contains 1 fl oz (30 ml) topical analgesic. Label includes Drug Facts panel listing Lidocaine 4% as the active ingredient. Manufactured by Transdermal Corporation, Birmingham, MI, USA.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.