Barr Hill Hand Sanitizer
Product Images NDC 75805-100

3 FDA label images from Caledonia Spirits Inc. · 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 Barr Hill Hand Sanitizer (NDC 75805-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Caledonia Spirits 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.

Product Images & Figures Index

FDA Label Image

1 (147ml Label)

1 (147ml Label)
Label for Barr Hill Hand Sanitizer, an alcohol antiseptic 80% topical solution in a 5 oz (147.9 ml) non-sterile bottle. The label states it follows the World Health Organization formulation and is produced by Caledonia Spirits Inc., Montpelier, Vermont. The back label shows drug facts including active ingredient, warnings, directions, and storage information, along with a barcode.*
FDA Label Image

3 (236ml Label)

3 (236ml Label)
Label for Barr Hill Hand Sanitizer, an alcohol antiseptic topical solution with 80% alcohol content. The 8 oz (236.6 ml) bottle label indicates it is a World Health Organization formulation and a non-sterile solution, produced by Caledonia Spirits Inc. in Montpelier, Vermont. The label includes usage, warnings, directions, and inactive ingredient information.*
FDA Label Image

2 (Label)

2 (Label)
Drug facts panel for Barr Hill Hand Sanitizer by Caledonia Spirits Inc., showing active ingredient as 80% alcohol with antiseptic purpose. It includes warnings about flammability, use restrictions, and keeping out of reach of children. Directions for use and storage information are also provided. Inactive ingredients include glycerol, hydrogen peroxide, and 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.