Gustar Hand Sanitizer (ethanol)
Product Images NDC 73819-0003

3 FDA label images from Gustar Co Ltd · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Gustar Hand Sanitizer (ethanol) (NDC 73819-0003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gustar 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 Tube

100 Tube
The label for Gustar Hand Sanitizer Gel features 70% alcohol content and claims to kill 99.9% of germs. It is a 3.3 fl. oz (100 ml) bottle made in Korea by GuStar Co Ltd. The label includes Drug Facts with active ingredient Ethyl alcohol 70% as an antiseptic, usage instructions, warnings, inactive ingredients, and distributor information.*
FDA Label Image

40 Pouch

40 Pouch
Front and back packaging labels of GUSTAR HAND SANITIZER (ETHANOL) by GuStar Co Ltd. The front label features the product name, a hand and droplet graphic, and size of 40 ml (1.35 fl. oz) with Korean text. The back label provides Drug Facts, active ingredient Ethyl alcohol 70%, usage, warnings, directions, inactive ingredients, product origin Korea, and distributor information.*
FDA Label Image

500 Bottle

500 Bottle
Label for Gustar Hand Sanitizer Gel, 16.9 fl. oz. (500 ml), containing 70% ethyl alcohol as the active ingredient. The label includes branding with the statements "Easily Anytime, Anywhere," "Smart Clean without Water and Soap," and emphasizes its antiseptic purpose. The label also features instructions, warnings, inactive ingredients including Aloe Vera Gel and Purified Water, and distributor information for GuStar Co. Ltd, Made in Korea.*

* 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.