American Hand Sanitizer
Product Images NDC 79421-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for American Hand Sanitizer (NDC 79421-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Hand Sanitizer, 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 1 Gallon Bzk)

Label of American Hand Sanitizer by American Hand Sanitizer LLC. It is a 1 gallon (3.8L) container of hand sanitizer with 0.13% Benzalkonium Chloride as the active ingredient. The label states it kills more than 99% of germs, leaves hands feeling soft, and includes Drug Facts such as uses, warnings, directions, and inactive ingredients. The product is made in the USA.*

FDA Label Image

Label 2 (Label 1 Shot Bzk)

Label for American Hand Sanitizer, showing the brand name prominently in red and blue. The product is alcohol-free and contains benzalkonium chloride 0.13%. It comes in 100 single-use packets, each packet containing 0.05 fl oz (1.5 ml), totaling 5 fl oz (150 ml). The label emphasizes germ-killing effectiveness and leaves hands feeling clean, with an icon of sanitizer being poured onto hands.*

FDA Label Image

Label 3 (Label 1 Shot Bzk)

Drug Facts panel for American Hand Sanitizer showing active ingredient Benzalkonium Chloride 0.13% as antiseptic. Includes uses for hand sanitizing to decrease bacteria and viruses, warnings for external use, instructions for use, inactive ingredients (Glycerin, Hydrogen Peroxide, Water), and distributor information for American Hand Sanitizer, LLC, made in USA. Also contains a barcode.*

* 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.