Xenoview Gas
Product Images NDC 80534-0750

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Xenoview (NDC 80534-0750). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Polarean, 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

Dose Delivery Bag (Xenoview 1)

Label for XENOVIEW (xenon Xe 129 hyperpolarized) gas for oral inhalation. It includes patient information fields, Xenon volume measurement, preparation details, and dose equivalent guidance. The label advises discarding XENOVIEW 60 minutes after bag filling and administering the dose within 5 minutes. Manufactured for Polarean, Inc., with storage instructions and NDC 80534-1000-1.*

FDA Label Image

Dose Delivery Bag Carton (Xenoview 2)

XENOVIEW (xenon Xe 129 hyperpolarized) dose delivery bags for oral inhalation by Polarean, Inc. The label indicates individual dose delivery bags compatible with the Polarean HPX System, including contents like 50 one-liter dose delivery bags, mouthpiece assemblies, individual dose labels, and prescribing information. The image features multiple label views and a photographic depiction of a dose delivery bag with a mouthpiece.*

FDA Label Image

Gas Cylinder Label (Xenoview 3)

Label for XENOVIEW xenon Xe 129 hyperpolarized gas blend for hyperpolarization, inhalation use. It lists gas components with concentrations: Xenon 1%, Nitrogen 10%, Helium 89%, and notes Xenon Xe 129 content >80%. Manufacturer is Polarean, Inc. The label includes safety and storage instructions, volume of 6,350 liters, and a barcode with NDC 80534-6350-1.*

* 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.