Axiv Sinus Severe Ultra Fine Mist Aerosol, Spray
Product Images NDC 82706-030

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Axiv Sinus Severe Ultra Fine Mist (NDC 82706-030). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vivunt Pharma 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

Directions (Directions For Use)

An instructional diagram showing how to use the AXIV Sinus Severe Ultra Fine Mist nasal spray. It depicts fingers holding the white tabs and squeezing the grooved area of the cap firmly while turning it counterclockwise to remove or secure the cap. The arrows indicate the direction for squeezing and turning.*

FDA Label Image

Principal Display Panel (Estuche Axiv Oxymetazoline Rev. 1 001)

Packaging label for AXIV Sinus Severe Ultra Fine Mist nasal spray, containing oxymetazoline hydrochloride 0.05% (0.5 mg/mL). The aerosol spray provides fast congestion relief with no drip, up to 265 sprays per 15 mL bottle. Distributed by Vivunt Pharma LLC, the label features usage instructions and drug facts indicating nasal decongestant use and warnings.*

FDA Label Image

Inner (Etiqueta Axiv Oxymetazoline Rev. 1 001)

Label for AXIV Sinus Severe Ultra Fine Mist nasal spray, containing oxymetazoline hydrochloride 0.05% in a 0.5 fl oz (15 ml) aerosol bottle. The label highlights maximum strength, up to 265 sprays, and 12-hour relief for nasal congestion and upper airway decongestion. It also includes drug facts, active ingredient, purpose, warnings, directions, and inactive ingredients. Distributed by VIVUNT PHARMA LLC.*

* 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.