Liberty Sanitizing Hand Liquid
Product Images NDC 73809-8059

6 FDA label images from Surry Chemicals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Liberty Sanitizing Hand Liquid (NDC 73809-8059). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Surry Chemicals Inc., 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

275 Gallon/1048.988l Label (Hand Sanitizer Label 275 Gals)

275 Gallon/1048.988l Label (Hand Sanitizer Label 275 Gals)
Drug Facts panel for Liberty Sanitizing Hand Liquid showing active ingredient Ethyl Alcohol 80% as antiseptic. Includes usage instructions for reducing bacteria on skin, warnings about flammability and external use, directions for applying the product, storage information, and a list of inactive ingredients: glycerin, hydrogen peroxide, purified water USP. The panel references manufacturing according to FDA temporary policy and USP grade ingredients.*
FDA Label Image

55 Gallon/208.198l Label (Hand Sanitizer Label 55 Gals)

55 Gallon/208.198l Label (Hand Sanitizer Label 55 Gals)
The image contains a full Drug Facts label for Liberty Sanitizing Hand Liquid, including active ingredient Ethyl Alcohol 80% as antiseptic, uses for reducing bacteria, warnings about flammability and external use, directions for use, storage information, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water. It mentions compliance with Temporary Policy for certain sanitizer products during COVID-19.*
FDA Label Image

5 Gallon/18.927l Label (Hand Sanitizer Label 5 Gals)

5 Gallon/18.927l Label (Hand Sanitizer Label 5 Gals)
Drug Facts panel for Liberty Sanitizing Hand Liquid displaying active ingredient Ethyl Alcohol 80% as antiseptic, usage instructions, warnings including flammability and external use only, directions for application, storage recommendations, and inactive ingredients such as glycerin, hydrogen peroxide, and purified water USP. The label references compliance with COVID-19 related temporary policies and WHO guidelines and includes a stylized Liberty logo with product size 5 gallons (18.93 liters).*
FDA Label Image

1 Gallon/3.785l Label (Hand Sanitzer Label 1 Gal)

1 Gallon/3.785l Label (Hand Sanitzer Label 1 Gal)
Drug Facts and product information panel for Liberty Sanitizing Hand Liquid. It specifies active ingredient ethyl alcohol 80%, use instructions, warnings including flammability and external use only, directions for application, storage instructions, and inactive ingredients glycerin, hydrogen peroxide, and purified water USP. The label mentions manufacture according to temporary FDA guidance and WHO recommendations for hand sanitizers.*
FDA Label Image

Lbg931 Liberty Hand Sani Liquid Front 2

Lbg931   Liberty Hand Sani   Liquid   Front 2
Label of Liberty Sanitizing Hand Liquid 64 fluid ounce (1.89 liters) bottle by Surry Chemicals Inc. The label features a stylized American flag design above the product name and states "Made in America" with the slogan "Let freedom clean!" The product NDC number 73809-8059-5 is visible at the bottom.*
FDA Label Image

Lbg932 Liberty Hand Sani Liquid Back 2

Lbg932   Liberty Hand Sani   Liquid   Back 2
Label of Liberty Sanitizing Hand Liquid by Surry Chemicals Inc. The label includes detailed Drug Facts listing ethyl alcohol 80% as the active ingredient with antiseptic purpose, along with warnings, directions, storage information, and inactive ingredients glycerin, hydrogen peroxide, and purified water USP. The product is positioned as a hand sanitizer adhering to regulatory guidance for alcohol-based sanitizers during the public health emergency.*

* 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.