Jublia Solution
Product Images NDC 0187-5400

6 FDA label images from Bausch Health Us Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Jublia (NDC 0187-5400). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch Health Us 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

Jublia Chemical Structure (Image 01)

Jublia Chemical Structure (Image 01)
Chemical structure of efinaconazole, the active ingredient in JUBLIA topical solution 100 mg/mL. The image shows the molecular structure with its associated molecular formula C18H22F2N4O and molecular weight 348.39.*
FDA Label Image

Image 02

Image 02
An instructional illustration showing a hand removing or placing a cap on a dropper bottle, demonstrating how to open or close the container for topical solution application.*
FDA Label Image

Image 03

Image 03
An instructional illustration showing a hand applying JUBLIA (efinaconazole) topical solution to a toenail. The image depicts the solution being dropped from the applicator directly onto the nail surface.*
FDA Label Image

Image 04

Image 04
An instructional illustration showing the application tip of a topical solution applicator positioned near the end of a toenail, indicating where to apply the medication.*
FDA Label Image

Image 05

Image 05
An instructional line drawing illustrating the application of a topical solution from a small bottle onto a toenail. The image shows a hand holding the bottle and dispensing the liquid onto the toenail of a foot, suggesting the use of the medication for toenail treatment.*
FDA Label Image

Image 06

Image 06
Packaging label for JUBLIA (efinaconazole) Topical Solution, 10%, 4 mL, distributed by Bausch Health US, LLC. The label includes active ingredient strength (100 mg/g) and contains usage warnings such as 'For Topical Use Only' and 'Not for use in eyes.' It provides storage instructions and a barcode. Manufactured by Bausch Health Companies Inc., Canada, with multiple U.S. patent numbers listed. The label features the Ortho Dermatologics logo and notes flammability warnings.*

* 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.