Ehsp Hand Sanitizer Wipe
Product Images NDC 82006-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ehsp Hand Sanitizer Wipe (NDC 82006-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ecep Han Medikal Tekstil Sanayi Ve Ticaret Limited Sirketi, 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

Label (Label)

The EHSP Hand Sanitizer Plus wipe packaging label features brand name and product description as an antiseptic hand sanitizer with 78.5% ethyl alcohol for hand disinfection. It includes bilingual drug facts, warnings, ingredients listing ethanol, glycerol, and aloe vera, and directions for use. The label shows manufacturer and contact details, a barcode, safety symbols, and highlights no sticky feeling and no rinse needed.*

FDA Label Image

Label2 (Label2)

EHSP Hand Sanitizer Wipe packaging label showing 10 wipes infused with 78.5% ethyl alcohol for hand disinfection. The label displays the EHSP logo and highlights aloe vera as an ingredient. It includes bilingual text in English and Spanish regarding use, warnings, and ingredients. The label is produced by ECEP HAN MEDIKAL TEKSTIL SANAYI VE TICARET LIMITED SIRKETI.*

FDA Label Image

Label3 (Label3)

EHSP Hand Sanitizer Plus Wipe packaging label from ECEP HAN MEDIKAL TEKSTIL SANAYI VE TICARET LIMITED SIRKETI. The label indicates 70 wipes per package with 78.5% ethyl alcohol as the active ingredient. The packaging features a green aloe vera leaf graphic and highlights hand disinfection and germ killing properties. Text is bilingual in English and Spanish, and the product is made in Turkey.*

* 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.