Hand Sanitizer (who Alcohol)
Product Images NDC 78590-100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (who Alcohol) (NDC 78590-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vigon International, Inc., 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

4 Jug Carton Label (Ndc 78580 100 02)

Drug fact label for Alcohol Based Handrub with W.H.O. recommended formulation. Manufactured by Vigon International, the label details a 4 gallon (4x1 gallon) container, usage instructions to apply a palmful and rub until dry, and warnings including flammability and caution to avoid eyes and keep away from children. It lists ingredients such as ethyl alcohol 78.3%, hydrogen peroxide 0.125%, and glycerol 2.16%, with a production date of 06/02/2020.*

FDA Label Image

Employee Use Pump Bottle (internal) (Ndc 78580 100 03)

Label for Hand Sanitizer (WHO Alcohol) by Vigon International, Inc. It is an alcohol-based hand rub formulated according to the World Health Organization. The label lists active ingredients including Ethyl Alcohol 79.83%, Water 13.07%, Hydrogen Peroxide 0.93%, and Glycerol 2.16%. The NDC is 78590-100-03.*

FDA Label Image

Bottle Label (Pckge 78590 100 01)

Label for Hand Sanitizer (WHO Alcohol) manufactured by Vigon International, Inc. The label states it is an alcohol-based handrub of 1 gallon volume following WHO recommended formulation. It lists active ingredients: Ethyl Alcohol 79.83%, Water 13.07%, Hydrogen Peroxide 3% at 4.93%, and Glycerol 2.16%. Safety instructions and hazard symbols for flammability and irritation are included. The label also provides manufacturer address in East Stroudsburg, PA.*

* 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.