Black Diamond Distillery Hand Sanitizer
Product Images NDC 74815-0001

2 FDA label images from Hocking Technical College · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Black Diamond Distillery Hand Sanitizer (NDC 74815-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hocking Technical College, 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

Active Ingredients (Hand Sanitizer For Fda Application Drug Facts)

Active Ingredients (Hand Sanitizer For Fda Application   Drug Facts)
Drug Facts panel for Black Diamond Distillery Hand Sanitizer shows active ingredient as Alcohol 80% v/v with antiseptic purpose. It details uses for reducing bacteria when soap and water are unavailable, warnings about flammability and age restrictions, directions for use, storage guidelines, and lists inactive ingredients including glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

Package Label Principal Display Panel (Hand Sanitizer For Fda Application Front Label)

Package Label Principal Display Panel (Hand Sanitizer For Fda Application   Front Label)
Label for Black Diamond Distillery Hand Sanitizer manufactured by Hocking Technical College, displaying 80% alcohol antiseptic topical solution. The label indicates it is a WHO recommended antiseptic hand rub formulation #1, for external use only, not safe for consumption, non-sterile solution, in a 1 gallon (3785.41 mL) container. It includes the manufacturer's address in New Straitsville, Ohio, and has space for date and batch information with an expiration of 30 days from the date noted.*

* 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.