Neomycin And Polymyxin B Sulfates And Bacitracin Zinc Ointment
Product Images NDC 24208-780

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 Bacitracin Zinc (NDC 24208-780). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bausch & Lomb Incorporated, 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

Image 01

Chemical structure diagram of neamine and neomycin (B and C) components, showing their molecular formula including functional groups and atomic connectivity. The structure also indicates the sulfate salt form with H2SO4.*

FDA Label Image

Image 02

Chemical structure diagram showing part of the molecular structure of Polymyxin B, including the sequence of amino acids and notation for sulfation (xH2SO4). Additional text identifies components such as DAB (2,4-diaminobutyric acid) and methylheptyl groups associated with Polymyxin B1R and B2R.*

FDA Label Image

Image 03

Chemical structure diagram illustrating a peptide or amino acid sequence with labeled residues and a connected heterocyclic ring structure. The diagram shows stereochemistry with D- and L- amino acid annotations, and a series of chemical bonds linking the components.*

FDA Label Image

Image 04

Packaging label for Neomycin and Polymyxin B Sulfates and Bacitracin Zinc Ophthalmic Ointment, USP (Sterile), 3.5 g tube by Bausch & Lomb Incorporated. The label includes active ingredient strengths, storage instructions, warnings, and usage directions. It features the NDC 24208-780-55 and states the product is for ophthalmic use only and Rx only.*

* 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.