Medi-first Burn With Lidocaine Cream
Product Images NDC 47682-270

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Medi-first Burn With Lidocaine (NDC 47682-270). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unifirst First Aid Corporation, 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

20669 (20669 Burn Cream Water Jel 3 8 21 1)

20669 (20669 Burn Cream Water Jel 3 8 21 1)
This image displays the Drug Facts and product label panels for Medi-First Plus Burn Cream with Lidocaine. The Drug Facts include active ingredients benzalkonium chloride 0.13% and lidocaine HCl 0.5%, along with their purposes as a first aid antiseptic and external analgesic. It lists uses, warnings, directions for use, storage instructions, inactive ingredients, and contact information. The product label shows the brand name with strength details, packaging quantity of 10 units, and net weight 0.9 g (1/32 oz), labeled by Unifirst First Aid Corporation.*
FDA Label Image

93973 (93973 Burn Cream Water Jel 3 8 21 2)

93973 (93973 Burn Cream Water Jel 3 8 21 2)
Drug Facts panel for Medi-First Plus Burn Cream with Lidocaine topical cream. It includes warnings before use such as avoiding deep wounds and animal bites, directions for use in adults and children over 2 years, storage and tamper information, inactive ingredients list, active ingredients and purposes, indications for first aid use, and safety warnings against use in eyes or on large areas. Manufacturer information for Medique Products is also present.*

* 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.