Floraseptic Wound Gel
Product Images NDC 52261-0602

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Floraseptic Wound Gel (NDC 52261-0602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cosco International, Inc., 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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FDA Label Image

3oz Tube Label (Floraseptic Hydrogel Label)

3oz Tube Label (Floraseptic Hydrogel Label)
This is a description of an antimicrobial hydrogel wound treatment product. It contains Benzethonium Chloride and Allantoin as active ingredients which work as an antiseptic and skin protectant respectively. The hydrogel is aimed to promote healing of minor cuts, scrapes, burns, and wounds, including pressure sores, diabetic ulcers, cracked skin and lips, and also helps decrease the risk of skin infection. The gel should be applied only to the affected area, 1 to 3 times daily, after cleaning the wound properly. It is not recommended to use it over large areas of the body, deep or puncture wounds, serious burns, deep cuts, animal bites, or in the eyes. Inactive ingredients include Aloe Barbadensis Leaf Juice, Ethanol, Hydrastis Canadensis L., Laureth-7, and Water among others. The product is made by BonePharm, LLC in the USA and comes in a 3 oz. (85g) package.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.