Hand Sanitizer
Product Images NDC 77941-500

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 77941-500). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blind Industries And Services Of Maryland, 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

236 mL Label (236ml Label)

Miracle Health Hand Sanitizer Gel with Aloe is an antimicrobial gel that helps reduce bacteria and viruses on the skin that can cause disease. It is recommended for repeated use and for external use only. It is flammable and should be kept away from heat and flames. If ingested, one should contact medical help or poison control center immediately. Not recommended for infants and children under 6 should be supervised when using it. It kills 99.9% of germs and has inactive ingredients such as water, aloe vera juice, glycerin, and lavender. Miracle Health Company LLC sells it and is located in Raleigh, NC.*

FDA Label Image

500 mL Label (500ml Label)

This is a description of a hand sanitizer gel with aloe, which contains Ethyl Alcohol 70% as an active ingredient. The purpose of this gel is to reduce bacteria and viruses on the skin and prevent diseases. It is not recommended for infants, and children under 6 years of age should be supervised when using it. It is flammable, so it should be kept away from fire or flame. If irritation or rash occurs, stop using it and see a doctor. If swallowed, seek medical help immediately. The gel needs to be rubbed on hands until it dries out. It is a product of Miracle Health Company LLC located in Raleigh, NC.*

* 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.