Hand Sanitizer
Product Images NDC 75104-001

3 FDA label images from Grey Skies 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 75104-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grey Skies 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

237ml Label (8oz42)

237ml Label (8oz42)
Drug Facts panel for Hand Sanitizer from Grey Skies Distillery, featuring active ingredient Alcohol 80% v/v as an antiseptic. Includes uses, warnings, directions for use, storage information, and inactive ingredients glycerin, hydrogen peroxide, and purified water USP. The text covers safety instructions and proper application guidelines.*
FDA Label Image

3785ml Rear Label (Hand Sanitizer Drug Facts Jpg)

3785ml Rear Label (Hand Sanitizer Drug Facts Jpg)
Drug Facts label panel for Hand Sanitizer by Grey Skies Distillery showing active ingredient Alcohol 80% v/v as an antiseptic. The label includes usage instructions, warnings about flammability and external use, age restrictions, directions for use, storage conditions, and a list of inactive ingredients including glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

3785ml Front Label (Hand Sanitizer Front Label Jpg)

3785ml Front Label (Hand Sanitizer Front Label Jpg)
Label for Eastern Kille Distillery Hand Sanitizer alcohol antiseptic 80% topical solution. The product is a non-sterile 1 gallon (3785.41 mL) solution. The design includes bold black text on a white background with a decorative logo below the main product name. Labeler is Grey Skies Distillery.*

* 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.