Hand Sanitizer
Product Images NDC 77797-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 77797-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grupo Plast-y-kosas, S.a. De C.v., 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

1 Gal Jalisco

Drug Facts label panel for Hand Sanitizer by Grupo Plast-Y-Kosas, S.A. de C.V. Lists active ingredient as Ethyl Alcohol 80% v/v with antiseptic purpose. Includes uses, warnings such as flammability and external use only, directions for application, storage instructions, and inactive ingredients including glycerin and hydrogen peroxide. Contains distributor and manufacturer information and volume of 128 oz (3,785 ml).*

FDA Label Image

1 Gal Pyk Mdk (1 Gal Pyk Mdk)

Drug Facts panel for Hand Sanitizer with 80% Ethyl Alcohol as the active antiseptic ingredient. The panel includes uses to reduce bacteria, warnings about external use and flammability, directions for use, storage information, and lists inactive ingredients such as glycerin and hydrogen peroxide. Safety advice and precautions for children are also provided.*

FDA Label Image

Master 8 Oz Ok Pharmacy

Drug Facts panel for Hand Sanitizer by Grupo Plast-Y-Kosas, S.A. de C.V., indicating the active ingredient as Ethyl Alcohol 80% v/v. The text includes purpose, use, warnings, directions, storage information, and inactive ingredients. It advises external use only, flammability caution, and to keep out of reach of children. The label also provides instructions for use and storage, as well as emergency contact recommendations.*

* 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.