Verasteril Advanced Hand Sanitizer
Product Images NDC 79236-000

3 FDA label images from Euroclydon Laboratories Usa Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Verasteril Advanced Hand Sanitizer (NDC 79236-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Euroclydon Laboratories Usa 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

Label (Label)

Label (Label)
Verasteril Advanced Hand Sanitizer packaging label with 75% Isopropyl Alcohol antiseptic in a topical, non-sterile gel form. The label highlights its antibacterial effectiveness and skin-softening properties. Distributed by Euroclydon Laboratories USA LLC, made in Mexico, with a net volume of 127.8 FL OZ (3780 ml).*
FDA Label Image

Label2 (Label2)

Label2 (Label2)
Verasteril Advanced Hand Sanitizer refreshing gel topical solution with 75% isopropyl alcohol antiseptic strength is shown in a 16.9 fluid ounce (500 ml) container. The label highlights it kills more than 99.9% of illness-causing germs, leaves hands feeling soft, and is distributed by Euroclydon Labs USA LLC, Katy, TX, made in Mexico.*
FDA Label Image

Label3 (Label3)

Label3 (Label3)
Drug Facts panel for Verasteril Advanced Hand Sanitizer Refreshing Gel, containing 75% isopropyl alcohol as the active ingredient with antiseptic purpose. The panel includes uses, warnings, directions, storage instructions, and inactive ingredients details. The label also mentions the product size as 2 FL OZ (60 ml) and distribution by Euroclydon Labs USA LLC, made in Mexico.*

* 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.