Clean On Hand Sanitizer
Product Images NDC 74522-010

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Clean On Hand Sanitizer (NDC 74522-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Caolion Cosmetics 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

Image Of Container (30 Container)

Label for CLEAN ON HAND SANITIZER gel containing 62% ethanol, offered in a 30 ml bottle by Caolion Cosmetics Co., Ltd. The label includes drug facts such as active ingredient concentration, warnings, directions, and manufacturer details. It also features a blue and white design with Korean and English text, a barcode, and product origin information (Made in Korea).*

FDA Label Image

Image Of Container (300 Container)

Drug Facts panel for Clean On Hand Sanitizer Gel showing active ingredient as Alcohol 62.0% w/w with purpose as sanitizer. The panel includes uses, warnings, directions, storage instructions, inactive ingredients, manufacturer (Korea COSPACK Co., Ltd.) and distributor (Caolion Cosmetics Co., Ltd.) information. The product net volume is 300 ml, made in Korea.*

FDA Label Image

Image Of Carton (3ml 10ea Carton)

CLEAN ON HAND SANITIZER Hand Sanitizer Gel featuring 62% ethanol. The label shows a blue and white design with a shield logo and text in English and Korean. It lists the product volume as 3 ml and identifies Caolion Cosmetics Co., Ltd. as the distributor. The label includes a Drug Facts panel with active ingredient, uses, warnings, directions, and manufacturer details. The product is made in Korea and includes a barcode.*

* 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.