Hand Sanitizer
Product Images NDC 80391-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 80391-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by 425579 Alberta Ltd, 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

Hand Sanitizer 4000 mL Label (Hand Sanitizer 4000 mL Label Usa)

Hand Sanitizer Non-sterile Solution containing Isopropyl Alcohol Antiseptic 75% Topical Solution in a 4000 mL (1.05 US Gallon) container. The label includes drug facts with active ingredient isopropyl alcohol (75% v/v) as an antiseptic, directions, warnings, and inactive ingredients glycerin, hydrogen peroxide, and purified water USP. Manufactured by 425579 Alberta Ltd, Calgary, AB, Canada.*

FDA Label Image

Hand Sanitizer 500 mL Label (Hand Sanitizer 500 mL Label Usa)

Drug Facts panel for Hand Sanitizer with 75% isopropyl alcohol topical solution, 500 mL. It lists the active ingredient as isopropyl alcohol 75%, with uses for reducing bacteria when soap is unavailable. Includes warnings, directions for use, storage instructions, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water. Labeler is 425579 Alberta Ltd.*

FDA Label Image

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Drug Facts panel for Hand Sanitizer by 425579 Alberta Ltd, containing 75% isopropyl alcohol as the active ingredient. The text provides information on usage as a topical antiseptic to reduce bacteria, warnings against use in children under 2 months or on open wounds, directions for application, storage instructions, and inactive ingredients including glycerin, hydrogen peroxide, and purified water. A barcode and company contact details are also visible.*

* 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.