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

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)

This is a product description for an external analgesic burn cream that contains Lidocaine HCI 0.5% and Benzalkonium chioride 0.13%. The cream helps to provide temporary relief for pain and prevent infection for minor burns, scrapes, and bites. It is suitable and safe for use for adults and children above 2 years of age. Users are advised to contact a Poison Control Center immediately if the cream is ingested and avoid applying it too close to the eyes. The product comes in a package of 10 units with a net weight of 0.9g each.*

FDA Label Image

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

This is a drug fact sheet providing information for the Burn Cream with Lidocaine product. It is advised to consult a doctor before use and avoid using the product on deep or puncture wounds, animal bites or serious burns. The product contains various ingredients including Benzalkonium Chloride 0.13%, Lidocaine HCl 0.5%, and mineral oil. The cream should be applied on the affected area up to 3 times a day and covered with a sterile bandage. It is only for external usage and should not be used in the eyes or on large areas of the body. If symptoms persist for more than 7 days, it is recommended to report a serious adverse reaction or to contact the manufacturer's customer service.*

* 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.