Hand Sanitizing Wipes
Product Images NDC 71120-613

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizing Wipes (NDC 71120-613). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanit Technologies 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.

FDA Label Image

Durisan Wipes 160 (Durisan Hand Sanitizing Wipes 160)

Durisan Hand Sanitizing Wipes alcohol-free sanitizing towelettes, 160 wipes per package. The packaging highlights long-lasting, no odor properties and includes Drug Facts information noting Benzalkonium Chloride 0.1% as the active antiseptic ingredient. Manufactured by Sanit Technologies LLC, Sarasota, Florida. Directions and warnings for use are provided on the label.*

FDA Label Image

Durisan Wipes 240 (Durisan Hand Sanitizing Wipes 240)

Durisan Hand Sanitizing Wipes packaging label shows an alcohol-free, long-lasting, no odor formulation in a 240-count package. The active ingredient is Benzalkonium Chloride 0.1% as an antiseptic. The label includes directions for use, warnings, and inactive ingredients. Labeler is Sanit Technologies LLC based in Sarasota, Florida.*

FDA Label Image

Durisan Wipes 80 (Durisan Hand Sanitizing Wipes 80)

Durisan Hand Sanitizing Wipes packaging label showing alcohol-free, long-lasting, no odor sanitizing towelettes. Contains 80 wipes sized 6 by 6.75 inches. Label includes Drug Facts panel listing benzalkonium chloride 0.1% as the active ingredient antiseptic, usage directions, warnings, and inactive ingredients. Manufactured by Sanit Technologies LLC, Sarasota, Florida.*

* 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.