Mediwiper
Product Images NDC 73923-0100

View Photos of 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 Mediwiper (NDC 73923-0100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Firstcham 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 (108g 20ct Container)

Image Of Container (108g 20ct Container)
Mediwiper Hand & Surface Sanitizing Wipes packaging label by FIRSTCHAM CO., LTD. Alcohol-free formula, containing 20 wipes in a resealable container. The product kills 99.9% of bacteria with benzalkonium chloride as an active ingredient. Made in Korea, distributed by Yes Sales Inc. The label includes Drug Facts, directions, warnings, and barcode.*
FDA Label Image

Image Of Container (432g 80ct Container)

Image Of Container (432g 80ct Container)
Packaging label for Mediwiper antiseptic hand and surface sanitizing wipes, manufactured by FIRSTCHAM CO., LTD. The label highlights 80 wipes per container, claims to kill 99.9% of harmful bacteria, and lists benzalkonium chloride 0.1% as the active ingredient. The label also includes a Drug Facts panel with usage instructions and warnings.*
FDA Label Image

Image Of Container (54g 10ct Container)

Image Of Container (54g 10ct Container)
Drug Facts panel of Mediwiper hand and surface sanitizing wipes with active ingredient Benzalkonium Chloride 0.1% as an antiseptic. The panel includes usage instructions, warnings for external use only, and safety information. It also mentions the expiration date and lot number are on the product. This panel supplements the packaging label details.*

* 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.