Hand Sanitizer
Product Images NDC 74144-075

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74144-075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Industrial Oils Unlimited, 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

3785 mL Label (Hand Sanitizer 1 Gal 4.3.2020)

Drug Facts panel of Hand Sanitizer containing 75% isopropyl alcohol as the active ingredient by Industrial Oils Unlimited, LLC. The panel includes uses, warnings about flammability and age restrictions, directions for use, other storage information, and a list of inactive ingredients. The label also includes contact information and logos for Adjuvants Unlimited and Industrial Oils Unlimited, with a net contents statement of 1 gallon.*

FDA Label Image

355 mL Back Label (Hand Sanitizer 12 Oz Back 4.3.2020)

Drug Facts panel for Hand Sanitizer by INDUSTRIAL OILS UNLIMITED, LLC, listing isopropyl alcohol 75% v/v as the active ingredient with antiseptic purpose. The panel includes uses, warnings about flammability and safety, directions for use, storage information, and inactive ingredients glycerin, hydrogen peroxide, and purified water USP.*

FDA Label Image

355 mL Front Label (Hand Sanitizer 12 Oz Front 4.3.2020)

Label for Hand Sanitizer containing 75% Isopropyl Alcohol Antiseptic topical solution. The label shows logos for Adjuvants Unlimited and Industrial Oils Unlimited, LLC. The net contents are 12 oz. The background features a light blue gradient oval with the tagline 'Making a difference TOGETHER' in red and blue text.*

* 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.