Dermal Wound Cleanser Spray
Product Images NDC 69740-492

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Dermal Wound Cleanser (NDC 69740-492). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Smith & Nephew Medical Ltd., 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

Package Display (Bottle, Spray (473mL))

Label for Dermal Wound Cleanser spray, containing 16 fl. oz. (473 mL) with active ingredient benzethonium chloride 0.13%, manufactured by Smith & Nephew Medical Ltd. The label highlights its use as a first aid antiseptic for wound cleansing and infection risk reduction, and includes Drug Facts, inactive ingredients, lot and expiration placeholders, and contact information.*

FDA Label Image

Package Display (Bottle, Spray (236mL))

Label of Dermal Wound Cleanser spray with Benzethonium chloride 0.13%, an 8 fl. oz. (236 mL) topical first aid antiseptic. The label shows the product name, strength, volume, and active ingredient along with Smith & Nephew branding and contact information. It includes Drug Facts detailing uses, warnings, directions, inactive ingredients, and a customer service phone number.*

* 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.