Neomycin And Polymyxin B Sulfates And Hydrocortisone Otic Suspension
Product Images NDC 50090-6336

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Neomycin And Polymyxin B Sulfates And Hydrocortisone Otic Suspension (NDC 50090-6336). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Label Image (Lbl500906336)

Label Image (Lbl500906336)
Label for Neomycin and Polymyxin B Sulfates and Hydrocortisone Otic Suspension, a prescription otic suspension manufactured by A-S Medication Solutions. The label includes storage instructions to keep the product between 59 and 77 degrees Fahrenheit and the container size of 10 mL. It also displays the National Drug Code (NDC) 50090-6336 and a lot number and product number section.*
FDA Label Image

Struct1 (Struct1)

Struct1 (Struct1)
Chemical structure diagram showing the molecular structure of neomycin B and neomycin C, components of neomycin. The diagram includes atomic groups and substitutions distinguishing neomycin B and C, with a sulfate group (H2SO4) indicated.*
FDA Label Image

Struct2 (Struct2)

Struct2 (Struct2)
Chemical structure diagram depicting the peptidic structure of Polymyxin B1 and B2 with labeled amino acids and functional groups, including α,γ-Diaminobutyric acid (DAB). The structure differentiates R as CH3 for Polymyxin B1 and H for Polymyxin B2, showing the sulfate salt form (× H2SO4).*
FDA Label Image

Struct3 (Structer3)

Struct3 (Structer3)
Chemical structure diagram of the active ingredient hydrocortisone, showing its molecular formula C21H30O5 and molecular weight 362.46.*

* 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.