Sinus Severe Ultra Fine Mist Aerosol, Spray
Product Images NDC 82706-026

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sinus Severe Ultra Fine Mist (NDC 82706-026). 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 illustration for Sinus Severe Ultra Fine Mist nasal spray demonstrating how to use the cap. It shows a hand holding the white tabs and squeezing the grooved area of the cap firmly while turning counterclockwise. Text emphasizes squeezing grooves firmly and securing the cap after use.*

FDA Label Image

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

Packaging label for Sinus Severe Ultra Fine Mist nasal spray by Vivunt Pharma LLC. The product contains Oxymetazoline HCl 0.05% as the active ingredient, in a 0.5 fl oz (15 mL) bottle providing up to 265 sprays. The label highlights fast, powerful congestion relief with no drip and a maximum strength formula. Directions, warnings, and drug facts are included on the label.*

FDA Label Image

Inner (Etiqueta Axiv Oxymetazoline Rev. 1 001)

Sinus Severe Ultra Fine Mist nasal spray with oxymetazoline hydrochloride 0.05% active ingredient in a 0.5 fl oz (15 ml) aerosol spray bottle. Label highlights fast and powerful congestion relief, nasal decongestant, and maximum strength offering up to 265 sprays and provides 12-hour relief. Distributed by Vivunt Pharma LLC, the label includes drug facts, warnings, directions, and inactive ingredients.*

* 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.