Maxitrol Suspension
Product Images NDC 82667-100

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Maxitrol (NDC 82667-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Harrow Eye, 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

Maxitrol-suspension-01.jpg (Maxitrol Suspension 01)

FDA Label Image

The Structural Formula For Neomycin Sulfate (Maxitrol Suspension 02)

FDA Label Image

The Structural Formula For Polymyxin B Sulfate (Maxitrol Suspension 03)

FDA Label Image

Maxitrol-suspension-04.jpg (Maxitrol Suspension 04)

Maxitrol-suspension-04.jpg (Maxitrol Suspension 04)
This is a description for a topical ophthalmic solution called "Maxitrol". It is meant for use in the eyes only. The solution should be stored upright at temperatures between 15°C and 27°C (59°F and 80°F) and should be shaken well before use. The solution contains neomycin sulfate, polymyxin B sulfate, and dexamethasone as active ingredients. The inactive ingredients include banzalkonium chloride, hydrochloric acid and/or sodium hydroxide, hypromellose 2910, polysorbate 20, purified water, and sodium chloride. The solution is manufactured by Harrow Eye, LLC in Nashville, TN, USA.*

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