Hand Sanitizer
Product Images NDC 74822-001

7 FDA label images from Headframe Spirits Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74822-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Headframe 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.

FDA Label Image

100 mL Label Rear (Hand Sani Label 100ml Back)

100 mL Label Rear (Hand Sani Label 100ml Back)
Drug Facts panel for Hand Sanitizer by Headframe Spirits Inc. Lists active ingredient as Alcohol 80% v/v with antiseptic purpose. Includes warnings about external use, flammability, and usage restrictions for children under 2 months and on open wounds. Directions instruct applying product until dry, with supervision for children under 6 years. Storage guidelines and inactive ingredients glycerin, hydrogen peroxide, and purified water USP are noted.*
FDA Label Image

3785.41 mL Label (Hand Sani Labels 1 Gal)

3785.41 mL Label (Hand Sani Labels 1 Gal)
Drug Facts panel for an Alcohol Antiseptic 80% Topical Solution hand sanitizer, 3.79L (1 gallon) size from Headframe Spirits Inc. It lists the active ingredient as 80% alcohol with antiseptic purpose, detailed usage, warnings, directions, and other storage information. Inactive ingredients include glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

100 mL Label Front (Hand Sani Labels 100ml 2nd Batch Front)

100 mL Label Front (Hand Sani Labels 100ml 2nd Batch Front)
Label for Hand Sanitizer alcohol antiseptic solution, 80% strength, in a 100 mL topical solution format. It is an antiseptic hand rub non-sterile solution. The product is brought by Headframe Spirits, along with Berry Global and Rock & Reilly's as listed on the label.*
FDA Label Image

473.2 mL Label (Hand Sani Labels 16oz)

473.2 mL Label (Hand Sani Labels 16oz)
Label of Headframe Spirits Inc. Hand Sanitizer, an alcohol antiseptic topical solution with 80% alcohol content. It is an antiseptic hand rub, non-sterile solution in a 473 mL (16 oz) container. The label includes drug facts such as active ingredient, usage instructions, warnings, and manufacturer's logo.*
FDA Label Image

1022060.7 mL Label (Hand Sani Labels 270 Gal)

1022060.7 mL Label (Hand Sani Labels 270 Gal)
Drug Facts panel for an Alcohol Antiseptic 80% Topical Solution hand sanitizer by Headframe Spirits Inc. It lists the active ingredient as Alcohol 80% v/v with antiseptic purpose, usage instructions, warnings about flammability and age restrictions, directions for use, and inactive ingredients including glycerin, hydrogen peroxide, and purified water USP.*
FDA Label Image

208197.55 mL (Hand Sani Labels 55 Gal)

208197.55 mL (Hand Sani Labels 55 Gal)
Drug Facts panel for Hand Sanitizer alcohol antiseptic 80% topical solution by Headframe Spirits Inc. It includes active ingredient (Alcohol 80%), purposes, usage instructions, warnings about flammability and age restrictions, directions for use, storage information, and a list of inactive ingredients (glycerin, hydrogen peroxide, purified water).*
FDA Label Image

18927.05 mL Label (Hand Sani 5 Gal Bucket Label)

18927.05 mL Label (Hand Sani 5 Gal Bucket Label)
Drug Facts panel for Hand Sanitizer containing 80% Alcohol Antiseptic, 18927 mL (5 gallons) non-sterile topical solution by Headframe Spirits Inc. It includes active ingredient details, uses, warnings, directions for use, and inactive ingredients such as glycerin and hydrogen peroxide. The label emphasizes flammability and storage instructions.*

* 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.