Newtralize
Product Images NDC 75519-001

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Newtralize (NDC 75519-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Newpark Industrial Blending Solutions Llc, 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

001-01 320gal (001 01 320gal)

Label for NewTralize Instant Hand Sanitizer by Newpark Industrial Blending Solutions LLC. The label details hazard warnings, active ingredient Alcohol 70% v/v as antiseptic, usage, precautions, and D.O.T. information (UN1993) for this flammable liquid. Net content is 320 U.S. gallons, with storage and safety instructions provided.*

FDA Label Image

001-02 265gal (001 02 265gal)

Label for NewTralize Instant Hand Sanitizer by Newpark Industrial Blending Solutions LLC. The label displays the product name, warnings including flammability and eye irritation hazards, and directions for use. It lists the active ingredient as 70% alcohol by volume and includes safety and storage information. The label also shows the DOT hazard code UN1993 for flammable liquid.*

FDA Label Image

001-03 1gal (001 03 1gal)

NewTralize instant hand sanitizer packaging label from Newpark Industrial Blending Solutions LLC. The label displays the product name prominently with hazard warning symbols for flammability and irritation. It includes safety warnings, usage instructions, and drug facts noting alcohol 70% as the active ingredient with antiseptic purpose. Net content is 1 U.S. gallon (3.79 liters).*

* 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.