Burnaid Burn Gel
Product Images NDC 51121-035
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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Burnaid Burn Gel (NDC 51121-035). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Clear Healthcare Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
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Principal Display Panel (3.5 g Packet Label)
This is a drug fact label for Burnaid burn gel. The active ingredient in the gel is Melaleuca 0il at 10mg/g concentration. The purpose of the gel is to treat minor burns, scalds, and sunburn. Users should not use the gel on serious burns and should discontinue use if irritation occurs. Inactive ingredients in the gel include Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Lactic Acid, PEG 7 Glyceryl Cocoate, Propylene Glycol, Purified Water, Tocopheryl Acetate, and Triethanolamine. The gel should be applied liberally to the affected area without rubbing it in and users should cover it if necessary. If pain persists, users should seek medical attention. The gel is for external use only and should not be stored at extreme temperatures. It is important to keep the gel out of reach of children and if swallowed, users should contact a Poison Control Center or get medical help right away. The NDC (National Drug Code) for the product is 51121-035-12.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.