Kovanaze
Product Images NDC 69803-100

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Kovanaze (NDC 69803-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by St. Renatus, 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

Tetracaine Hydrochloride Structural Formula (Kov00 0000 01)

Tetracaine Hydrochloride Structural Formula (Kov00 0000 01)
Chemical structure diagram of the active ingredient in Kovanaze, showing the molecular arrangement including a phenyl group, carbamate, and amine functional groups, along with an associated hydrochloride (HCl) moiety.*
FDA Label Image

Oxymetazoline Hydrochloride Structural Formula (Kov00 0000 02)

Oxymetazoline Hydrochloride Structural Formula (Kov00 0000 02)
Chemical structure of Kovanaze active ingredient, depicted with chemical group notations including hydroxyl, methyl, and an imidazole ring, alongside HCl indicating hydrochloride salt form.*
FDA Label Image

Principal Display Panel (Box Label)

Principal Display Panel (Box Label)
Kovanaze nasal spray packaging label showing the product name with active ingredients tetracaine HCl and oxymetazoline HCl. The label indicates a 0.2 mL spray volume, containing 6 mg tetracaine HCl and 0.1 mg oxymetazoline HCl per spray, equivalent to 5.27 mg tetracaine and 0.088 mg oxymetazoline. The package contains 30 sprays, labeled for professional use in dentistry, manufactured by St. Renatus, LLC in Fort Collins, CO. Storage instructions specify refrigeration at 2 to 8°C (36 to 46°F).*

* 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.