Hand Sanitizer
Product Images NDC 76542-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 76542-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Moon Chemical Products, 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 Label Moon Chemical

Drug Facts panel for Hand Sanitizer by Moon Chemical Products contains active ingredient Alcohol 80% with antiseptic purpose. It includes usage instructions, warnings such as flammability and external use only, directions for application, storage conditions, and inactive ingredients like glycerine, hydrogen peroxide, and purified water. Contact information and company logo are also visible.*

FDA Label Image

100 mL Label (4 Oz Label Moon Chemical)

Drug facts panel for Hand Sanitizer by Moon Chemical Products, describing the active ingredient as 80% alcohol with antiseptic purpose. It includes use instructions, warnings about flammability and external use only, storage information, and inactive ingredients such as glycerine, hydrogen peroxide, and purified water. The panel emphasizes avoiding use in children under 2 months and on open wounds, and advises to keep out of reach of children.*

FDA Label Image

55 Gal Label Moon Chemical

Drug Facts label for Hand Sanitizer by Moon Chemical Products, featuring active ingredient Alcohol 80%. The label includes warnings, directions for use, and storage information. It also lists inactive ingredients as glycerine, hydrogen peroxide, and purified water. The label displays contact information for Moon Chemical Products in Oklahoma City, OK.*

* 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.