Instant Hand Sanitizer
Product Images NDC 73817-100

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Instant Hand Sanitizer (NDC 73817-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Screening 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-16oz (Label 16oz)

Label of Instant Hand Sanitizer by American Screening LLC showing 16 fl oz (473 ml) size. The product contains 70% ethyl alcohol as the active ingredient with antibacterial purpose. The label includes drug facts with warnings, directions, and inactive ingredients such as aloe, glycerin, and vitamin E. It features a moisturizing formula with aloe and a claim of killing 99.9% of germs.*

FDA Label Image

Label-4oz (Label 4oz)

Label for Instant Hand Sanitizer by American Screening LLC shows a 4 fl oz (118 ml) bottle size. The product highlights killing 99.9% of germs and features a moisturizing formula with aloe. The label includes a Drug Facts panel listing Ethyl Alcohol 70% as the active antibacterial ingredient and directions for use.*

FDA Label Image

Label-8oz (Label 8oz)

Label for Instant Hand Sanitizer by American Screening LLC with 70% Ethyl Alcohol as the active ingredient. The label highlights its antibacterial purpose, moisturizing formula with aloe, and net volume of 8 fl oz (236 ml). It includes Drug Facts with use, warnings, directions, and inactive ingredients listed, manufactured in the USA by American Screening LLC.*

* 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.