Natezone Hand Sanitizer
Product Images NDC 90010-901

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Natezone Hand Sanitizer (NDC 90010-901). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Guangzhou Cluster Mapping Supply Chain 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

Label 12 New

NateZone Hand Sanitizer Alcohol Antiseptic 75% Topical Solution 12 FL OZ (354 ml) bottle label. Features an orange and white design with the brand name, antibacterial and aloe gel claims. Includes active ingredient ethyl alcohol 75% and dispensing, warnings, directions, and inactive ingredients information. Manufactured by Guangzhou Cluster Mapping Supply Chain Co., Ltd and distributed by NateZone, Inc.*

FDA Label Image

Label 2 New

NateZone Hand Sanitizer label with Alcohol Antiseptic 75% Topical Solution. The label highlights antiseptic hand sanitizer with aloe gel, antibacterial properties, and a 2 FL OZ (60 ml) size. The product is labeled by Guangzhou Cluster Mapping Supply Chain Co., Ltd and distributed by NateZone, Inc, including drug facts, active ingredients, directions, warnings, and storage information.*

FDA Label Image

Label 8 New

NateZone Hand Sanitizer label showing Alcohol Antiseptic 75% Topical Solution in an 8 fl oz (236 ml) bottle. The label highlights antibacterial and aloe gel features. It includes drug facts with Ethyl Alcohol 75% as the active ingredient, warnings, directions, and inactive ingredients. Manufactured and distributed by Guangzhou Cluster Mapping Supply Chain Co., Ltd and NateZone, Inc.*

* 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.