Instant Hand Sanitizer
Product Images NDC 78801-075

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Instant Hand Sanitizer (NDC 78801-075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dura Micro 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

100ml Label (100ml Page 001)

Label for Instant Hand Sanitizer by Dura Micro Inc, containing 75% alcohol and aloe vera, in a 3.38 fl. oz (100 ml) dosage form. The label highlights that it kills 99.9% of bacteria, is for external use only, and includes detailed drug facts, warnings, directions, inactive ingredients, manufacturer and distributor information, and storage instructions. The product is made in China.*

FDA Label Image

500ml Label (500ml Page 001)

Label for Instant Hand Sanitizer by Dura Micro Inc, featuring 75% alcohol antiseptic hand sanitizer. The label highlights killing 99.9% bacteria, no rinse needed, aloe vera ingredient, and 16.91 fl.oz (500ml) volume. Manufacturer and distributor details, drug facts, usage warnings, directions, inactive ingredients, and barcode are included.*

FDA Label Image

50ml Label (50ml Page 001)

Label for Instant Hand Sanitizer by Dura Micro Inc, featuring 75% alcohol content and 50 ml (1.69 fl. oz) volume. The label highlights Aloe Vera and indicates the product kills 99.9% bacteria. Directions, warnings including flammability, and external use instructions are provided. The label includes manufacturing and packaging details, a barcode, and batch and expiry date information.*

* 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.