Dermarite Antibacterial Wet Wipes
Product Images NDC 79770-001

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Dermarite Antibacterial Wet Wipes (NDC 79770-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Shaoxing Hengsheng New Material Technology Development Co., 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.

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FDA Label Image

11 (77850 002 75 Alcohol)

11 (77850 002 75 Alcohol)
This is a description of a hand sanitizer wipe that contains 75% ethyl alcohol, designed to decrease bacteria on the skin. This product is meant for external use only and should not be used in or near the eyes. It is intended for general cleaning purposes and does not replace wipes used during medical procedures. The product should be kept out of reach of children, stored below 95F(35C), and in a dry place away from fire. If irritation or redness develops, discontinue use and seek medical attention if it persists for over 72 hours. To use, the user should wet their hands with the product and allow to dry naturally without wiping. Inactive ingredients include purified water, glycerin, aloe Barbadensis extract, Phenoxyethanol, Ethylhexylglycerin, and Propylene Glycol.*

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