Liberty Hand Sanitizer Gel
Product Images NDC 73809-8067

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 Hand Sanitizer Gel (NDC 73809-8067). 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

1 Gallon/3.785 L (Liberty Gel Hand Sanitizer 61 1 Gal)

1 Gallon/3.785 L (Liberty Gel Hand Sanitizer 61 1 Gal)
Drug Facts panel for Liberty Hand Sanitizer Gel with active ingredient Ethyl Alcohol 61% as an antiseptic. Includes use, warnings about flammability and external use only, directions for application, storage information, and a list of inactive ingredients such as glycerin and hydrogen peroxide. Also shows branding with Liberty logo, product volume 1 gallon (3.785 liters), and labeler Surry Chemicals, Inc.*
FDA Label Image

5 Gallons/18.9l (Liberty Gel Hand Sanitizer 61 5 Gal)

5 Gallons/18.9l (Liberty Gel Hand Sanitizer 61 5 Gal)
Drug Facts panel for Liberty Hand Sanitizer Gel with active ingredient Ethyl Alcohol 61% as an antiseptic. Includes uses, warnings about flammability and external use, directions for application, storage instructions, and a list of inactive ingredients such as glycerin and hydrogen peroxide. The panel is accompanied by product branding stating 5 gallons (18.93 liters) and Made in America.*
FDA Label Image

55 Gallons/208 L (Liberty Hand Gel 61 55 Gal)

55 Gallons/208 L (Liberty Hand Gel 61 55 Gal)
Drug Facts panel for Liberty Hand Sanitizer Gel by Surry Chemicals, Inc. It lists ethyl alcohol 61% as the active ingredient and antiseptic purpose. The panel includes warnings about flammability, use restrictions, directions for application, and storage conditions. Inactive ingredients include glycerin, hydrogen peroxide, eucalyptus oil, trolamine, carbomer 940, and water. The image also includes the front label showing product name, volume (55 gallons), and "Made in America" statement.*
FDA Label Image

1.893l/ 0.5g Back (Liberty Hand Sanitizer 61 64oz Back2)

1.893l/ 0.5g Back (Liberty Hand Sanitizer 61 64oz Back2)
Drug Facts panel from Liberty Hand Sanitizer Gel by Surry Chemicals, Inc. The panel includes active ingredient (ethyl alcohol 65%), antiseptic purpose, usage instructions to reduce bacteria on the skin, warnings about flammability and proper use, directions for application, storage information, and lists inactive ingredients such as glycerin, hydrogen peroxide, eucalyptus oil, tromaine, carbomer 940, and water.*
FDA Label Image

1.893l/0.5 Gallon Front (Liberty Hand Sanitizer Label 61 64oz Front2)

1.893l/0.5 Gallon Front (Liberty Hand Sanitizer Label 61 64oz Front2)
The packaging label for Liberty Hand Sanitizer Gel by Surry Chemicals, Inc. is displayed on a clear bottle containing 64 fl oz (1.89 liters). The label features the brand name LIBERTY in large font with an abstract red and blue flag above it. The words HAND SANITIZER GEL are centered below the brand name, with MADE IN AMERICA and the slogan "Let freedom clean!" printed beneath in red and blue text. The product NDC 73809-8067-5 is shown at the bottom of the label.*
FDA Label Image

275 Gallon/1048l (Liberty Hand Gel 61 275 Gal)

275 Gallon/1048l (Liberty Hand Gel 61 275 Gal)
Drug Facts panel for Liberty Hand Sanitizer Gel showing active ingredient Ethyl Alcohol 61% as an antiseptic. The panel includes warnings about flammability and external use, directions for use, storage conditions, and lists inactive ingredients like glycerin and eucalyptus oil. The label also features the brand name with a graphic of a stylized flag and the tagline 'Let freedom clean!'.*

* 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.