Hand Sanitizer
Product Images NDC 74322-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74322-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mount Royal Soaps, 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

1 Gal 74322-001-03 (1gal Who Label 04022020)

Label for Hand Sanitizer by Mount Royal Soaps, LLC featuring a red and white checkered design with the text 'Mount Royal Soap Company'. It states 'Alcohol Antiseptic 80% Topical Solution' and 'Hand Sanitizer Non-Sterile Solution'. The container size is indicated as 1 gallon (3785 mL). The label includes drug facts such as active ingredient, uses, warnings, directions, and inactive ingredients. Contact information for the manufacturer and website mountroyalsoaps.com are also shown.*

FDA Label Image

2oz 74322-001-01 (2oz Who Label 04022020)

Drug Facts panel for Mount Royal Soaps Hand Sanitizer, 2 fl oz (59 ml) non-sterile topical solution containing 80% alcohol as the active ingredient. The label includes directions for use, warnings, inactive ingredients (glycerin, hydrogen peroxide, purified water), and contact information for Mount Royal Soaps, LLC, Baltimore, MD.*

FDA Label Image

4 Oz 74322-001-02 (4oz Who Label 04022020)

Label for Mount Royal Soaps LLC Hand Sanitizer 4 fl oz (118 mL) topical solution containing 80% v/v alcohol antiseptic. The label includes Drug Facts with active ingredient, uses, warnings, directions, and inactive ingredients (glycerin, hydrogen peroxide, purified water USP). The product is non-sterile and made in the USA.*

* 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.