Axiv Sinus Overnight Spray
Product Images NDC 82706-034

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Axiv Sinus Overnight (NDC 82706-034). 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

Bottle (Axiv Overnight Bottle)

AXIV Sinus OVERNIGHT nasal spray with Oxymetazoline HCl 0.05% active ingredient. The label describes it as a nasal decongestant for temporary relief of nasal congestion due to cold, hay fever, or other upper respiratory allergies. The 0.5 fl oz (15 ml) bottle is labeled non-drowsy and intended for overnight use. Distributed by Vivunt Pharma LLC.*

FDA Label Image

Directions (Directions For Use Oxy Overnight)

An instructional diagram showing how to use the cap of a nasal spray. It depicts a hand holding the grooved cap with the instruction to squeeze the grooved area firmly while turning the cap counterclockwise, with arrows indicating the direction of movement and pressure points to hold the tabs firmly.*

FDA Label Image

Pdp1 (Out Est. Axiv Oxymetazoline Overnight Copia 001)

The AXIV Sinus OVERNIGHT nasal spray carton displays the product name with active ingredient Oxymetazoline HCl 0.05%. It indicates 0.5 fl oz (15 ml) spray volume, offering 12 hours of relief with 265 sprays. Labeler is Vivunt Pharma LLC, with directions for use and drug facts panel visible on the sides. The packaging features a night-time theme with a crescent moon graphic.*

* 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.