Hand Sanitizer
Product Images NDC 74444-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 74444-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guangzhou Mizhuangmifang Biotechnology Co. , Ltd., 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 (Label 1)

The label for Hand sanitizer from Guangzhou Mizhuangmifang Biotechnology Co., Ltd. features a blue background with an image of two hands inside a white droplet shape. The label states the product contains Ethyl Alcohol 75.0% and includes warnings, directions, inactive ingredients, and manufacturer information. It has a volume of 3.52 FL. OZ (100ml) and a barcode at the bottom right.*

FDA Label Image

300 mL Label (Label 2)

Label for Hand sanitizer by Guangzhou Mizhuangmifang Biotechnology Co., Ltd. The product contains 10.56 fluid ounces (300 ml). The label lists inactive ingredients including ethanol and propanediol, and states ethyl alcohol at 75% as the active antimicrobial ingredient. Usage instructions, warnings, storage information, addresses for manufacturer and entrusted party, and a barcode are also shown.*

FDA Label Image

500 mL Label (Label 3)

Label of Hand Sanitizer by Guangzhou Mizhuangmifang Biotechnology Co., Ltd. The label includes active ingredient Ethyl Alcohol 75.0% as antimicrobial, and inactive ingredients like Ethanol and Carbomer. The product volume is 17.6 FL.OZ (500ml). The label contains usage directions, warnings, manufacturing and distribution information, barcode, and cautions about flammability and proper use.*

* 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.