Hand Sanitizer
Product Images NDC 75636-021

3 FDA label images from Boot Hill Distillery · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 75636-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Boot Hill Distillery, 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

9.5 L Label (2.5g Hand Sanitizer (1) (1))

9.5 L Label (2.5g Hand Sanitizer  (1) (1))
Drug Facts panel for Boot Hill Distillery Hand Sanitizer Non-Sterile Solution with 80% alcohol antiseptic. Includes active ingredient, intended use, warnings for external use and flammability, directions for use and supervision of children, storage instructions, and inactive ingredients glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

1000 L Label (264 G Label)

1000 L Label (264 G Label)
Drug Facts label for Boot Hill Distillery Hand Sanitizer Non-Sterile Solution showing active ingredient 80% alcohol as antiseptic. It includes warnings for external use, flammability, and instructions to keep away from eyes, ears, and mouth. Directions for use and storage information are provided, along with inactive ingredients glycerin, hydrogen peroxide, and purified water.*
FDA Label Image

90 mL Label (3oz Hand Sanitizer Copy)

90 mL Label (3oz Hand Sanitizer Copy)
Drug Facts panel for Hand Sanitizer Non-Sterile Solution by Boot Hill Distillery. The active ingredient is 80% alcohol as an antiseptic. It includes uses, warnings for external use, directions for application, and storage information. Inactive ingredients listed are glycerin, hydrogen peroxide, and purified water USP.*

* 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.