Lone Star Botanicals Hand Sanitizer Gel
Product Images NDC 81225-001

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Lone Star Botanicals Hand Sanitizer Gel (NDC 81225-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lone Star Botannicals, 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

355ml Gel Ndc: 81225-001-02 (Lsb12ag)

Drug Facts panel for Lone Star Botanicals Hand Sanitizer containing 80% alcohol antiseptic in a 12 oz (355 mL) non-sterile unscented aloe gel solution. The panel includes active ingredient, uses, warnings, directions, storage information, and inactive ingredients. Manufactured by Huck Diversified Technologies, LLC, Jacksonville, TX.*

FDA Label Image

355ml Gel (Scented NDC: 81225-001-05)

Drug Facts panel for Lone Star Botanicals Hand Sanitizer alcohol antiseptic 80%, scented gel. Contains warnings, directions for use, storage instructions, active ingredient (alcohol 80%), and a list of inactive ingredients such as cinnamon, clove, lemon, and eucalyptus. Manufactured by Huck Diversified Technologies, LLC in Jacksonville, TX.*

FDA Label Image

60ml Gel Ndc: 81225-001-01 (Lsb2ag)

Lone Star Botanicals Hand Sanitizer 80% Alcohol Antiseptic 2.0 oz (60 mL) non-sterile solution. The front label identifies it as an unscented aloe gel hand sanitizer manufactured by Lone Star Botanicals in Tyler, TX. The back label includes drug facts such as active ingredient (80% alcohol), uses, warnings, directions, storage instructions, and inactive ingredients.*

FDA Label Image

60ml Gel (Scented NDC: 81225-001-04)

The image shows the label of Lone Star Botanicals Hand Sanitizer, an alcohol antiseptic 80% scented gel in a 2.0 oz (60 mL) non-sterile solution. It is manufactured by Huck Diversified Technologies, LLC, located in Jacksonville, TX. The label includes a Drug Facts panel listing active and inactive ingredients, usage directions, warnings, and storage instructions.*

FDA Label Image

946ml Gel Ndc: 81225-001-03 (Lsb32ag)

Drug Facts label for Lone Star Botanicals Hand Sanitizer with 80% alcohol antiseptic in a non-sterile unscented aloe gel solution. It includes warnings, directions, storage instructions, and lists active ingredient as alcohol 80% w/w along with inactive ingredients such as aloe vera and glycerin. Manufacturer details for Huck Diversified Technologies, LLC are also shown.*

FDA Label Image

946ml Gel (Scented NDC: 81225-001-06)

Drug Facts panel for Lone Star Botanicals Hand Sanitizer, an 80% alcohol antiseptic scented gel non-sterile solution. It includes active ingredient information, uses, warnings about flammability and age restrictions, directions for use, storage conditions, and a list of inactive ingredients such as cinnamon and clove.*

FDA Label Image

120ml Spray Ndc: 81225-002-01 (Lsb4as)

Label for Lone Star Botanicals Hand Sanitizer, an unscented aloe spray alcohol antiseptic 80% non-sterile solution in a 4.0 oz (120 mL) bottle. Manufactured by Huck Diversified Technologies, LLC, located in Jacksonville, TX. The label includes drug facts, directions, warnings, and inactive ingredients.*

FDA Label Image

120ml Spray (Scented NDC: 81225-002-02)

Drug Facts label for Lone Star Botanicals Hand Sanitizer Alcohol Antiseptic 80% (Scented Spray), 4.0 oz (120 mL), manufactured by Huck Diversified Technologies, LLC. The label lists active ingredient alcohol 80% v/v as antiseptic, usage instructions, warnings, directions, storage conditions, and inactive ingredients including cinnamon, clove, lemon, eucalyptus, rosemary, glycerin, hydrogen peroxide, and purified water.*

* 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.