Polymyxin B Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-321

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Polymyxin B (NDC 63323-321). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structural Formulae (Pol0c 0000 01)

Chemical structure diagram showing polymyxin B with labels indicating different components of the molecule including Dab, Thr-Dab, Leu, and Phe groups. It illustrates the molecular arrangement and chemical bonds of the active ingredient polymyxin B sulfate.*

FDA Label Image

Fresenius Kabi Logo (Pol0c 0000 02)

FDA Label Image

Principal Display Panel – Vial Label (Pol0c 0000 03)

Label for Polymyxin B injection, USP 500,000 units per vial. Each sterile, lyophilized vial contains Polymyxin B sulfate equivalent to 500,000 units. The product is labeled for hospital use with multiple administration routes including intramuscular, intravenous, intrathecal, and ophthalmic. Manufacturer is Fresenius Kabi USA, LLC. The label includes dosage warnings, storage instructions before and after reconstitution, and notes that the product is Rx only.*

FDA Label Image

Principal Display Panel – Vial Tray (Pol0c 0000 04)

Polymyxin B for Injection, USP 500,000 units per vial label by Fresenius Kabi USA, LLC. The label states the product contains Polymyxin B Sulfate equivalent to 500,000 units, sterile, lyophilized powder for injection. It includes 10 sterile vials and indicates Rx only. Storage and usage warnings, routes of administration (intramuscular, intrathecal, intravenous, ophthalmic), and barcode are present.*

* 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.