Hand Sanitizer
Product Images NDC 76538-002

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 76538-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Elite Endeavors, Llc, 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

3785.41 mL (Mhm Gel Front Label)

3785.41 mL (Mhm Gel Front Label)
This appears to be a label for an alcohol-based antiseptic topical solution and hand sanitizer. The label indicates that it is a non-sterile solution and contains 807 alcohol. The product comes in a large container with a capacity of 3785.41 mL or 1 gallon.*
FDA Label Image

3785.41 mL (Mhm Gel Back Label)

3785.41 mL (Mhm Gel Back Label)
This text provides information about a hand sanitizer solution containing 80% alcohol as the active ingredient to help reduce bacteria that can cause disease when soap and water are not available. The product is flammable and should be kept away from heat or fire. It is not recommended for use in children under 2 months of age or on open skin wounds. The user should avoid contact with the eyes, ears, and mouth and contact a doctor if irritation or rash occurs. The product should be rubbed on hands thoroughly until dry, and it should not be swallowed. The product contains glycerin, polycacrylamide, hydrogen peroxide, purified water USP, and is manufactured by Elite Endeavors LLC and American Premiere Equine in Lexington, NE. The product's website is www.masterhandsanitizer.com.*
FDA Label Image

3785.41 mL Back Label (Mhm Back Label)

3785.41 mL Back Label (Mhm Back Label)
This is a drug facts label of a hand sanitizer. The active ingredient is 80% alcohol which is an antiseptic. It is used to help reduce bacteria that can potentially cause disease. The product is for external use only and should be kept away from heat and flame. It should not be used on children below 2 months or on open skin wounds. The user should avoid contact with eyes, ear, and mouth. The user should stop using the product if irritation or rash occurs. The product should be kept out of reach of children and if swallowed, medical help should be sought. To use the product, apply on the hands and rub them together until dry. Children under 6 years of age should be supervised while using the product. The product should be stored between 15-30 degrees Celsius and should be protected from freezing and heat above 40 degrees Celsius. The inactive ingredients are glycerin, hydrogen peroxide, and purified water. The hand sanitizer is manufactured by Elite Endeavors, LLC and American Premiere Equine in Lexington, NE.*
FDA Label Image

3785.41 mL Front Label (Mhm Front Label)

3785.41 mL Front Label (Mhm Front Label)
The text is not-readable and appears to be a combination of random characters and symbols.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.