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)

This is a description of an Alcohol Based Handrub product manufactured by Vigon International with NOC 7859010002. It contains 7983% Ethyl Alcohol and 1307% water. There is a mention of a recommended formula but it is not provided in the text.*

FDA Label Image

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

This text describes the formulation for an alcohol-based handrub, specifically the one recommended by the World Health Organization. It contains 79.83% Ethyl Alcohol, 13.07% Water, 4.93% Hydrogen Peroxide 3%, and 2.16% Glycerol. This information is likely useful for those looking to create their own handrub solutions.*

FDA Label Image

Bottle Label (Pckge 78590 100 01)

This is a WHO recommended formulation for an Alcohol Based Handrub manufactured by Vigon International. It is available in one-gallon size and is meant to be used for external purposes only. The product contains Ethyl Alcohol (79.83%), Water (13.07%), Hydrogen Peroxide 3% (493%), and Glycerol (216%). The user should apply a palmful of the product and cover all surfaces of their hands, rubbing until dry. It should be kept away from the reach of children and eyes. Also, it is flammable and must be kept away from heat and flame. The SDS provides further hazard information, and the product was produced on 06/02/2020.*

* 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.