Ketoconazole Aerosol, Foam
Product Images NDC 71335-2941

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Ketoconazole (NDC 71335-2941). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chemical Structure (Image 01)

FDA Label Image

Step-1.jpg (Image 02)

FDA Label Image

Step-2.jpg (Image 03)

FDA Label Image

Step-2.1.jpg (Image 04)

FDA Label Image

Step-3.jpg (Image 05)

FDA Label Image

Step-3.1.jpg (Image 06)

FDA Label Image

Step-4.jpg (Image 07)

FDA Label Image

Label (Lbl713352941)

This text provides essential information about a medication containing 20 mg of Ketoconazole, USP per gram. It emphasizes that the medication should only be used as prescribed by a physician and provides a warning that it is flammable, cautioning against exposure to fire, flame, or smoking during and after application. It specifies that the medication is for topical use only and advises against ophthalmic, oral, or intravaginal use. Additionally, the text instructs on proper storage conditions, including avoidance of high temperatures, direct sunlight, and puncturing the container. Manufacturer details are also provided.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.