Usualklenz Disinfectantspray
Product Images NDC 81057-302

2 FDA label images from Novawear Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Usualklenz Disinfectantspray (NDC 81057-302). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novawear 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

500ml Ndc: 81057-301-02 (Disinfectant Spray Label 500ml)

500ml Ndc: 81057-301-02 (Disinfectant Spray Label 500ml)
Label of USUALKLENZ DISINFECTANT SPRAY, an antimicrobial spray by NOVAWEAR INC. The product contains 500 ml (16.9 oz) and claims to kill 99.9% of viruses and bacteria. It is scent-free, ethanol-free, proven gentle on skin, with a skin irritation test passed, and made with 100% natural minerals. Directions and drug facts identify hydrogen peroxide as the active antimicrobial ingredient. The label also includes warnings, inactive ingredients, storage instructions, a barcode, and distributor information.*
FDA Label Image

60ml Ndc: 81057-301-01 (Disinfectant Spray Label 60ml)

60ml Ndc: 81057-301-01 (Disinfectant Spray Label 60ml)
Label for USUALKLENZ DISINFECTANT SPRAY by NOVAWEAR INC. The label highlights its antimicrobial properties, killing 99.9% of viruses and bacteria. It is a 60 mL (2 oz) spray, proven gentle on skin and eliminating odors. The product is scent-free, ethanol-free, contains 100% natural minerals, and has passed skin irritation tests. Directions and drug facts, including active ingredient hydrogen peroxide, are detailed. Made in Korea, distributed by Novawear 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.