Mannitol-structure (Man03 0000 01)
Chemical structure of Mannitol showing its molecular arrangement including hydroxyl groups and carbon atoms.*
Mannitol Injection, Solution
Product Images NDC 63323-024
5 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Mannitol (NDC 63323-024). 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.
Mannitol-image (Man03 0000 02)
This text panel titled 'PREPARATION OF DILUTIONS FOR INTRAVENOUS INJECTION' provides instructions for preparing different concentrations of mannitol solution from a 25% stock solution. It lists concentrations from 5% to 25% with corresponding preparation methods using specific volumes of mannitol and diluents, including a note about using 5% Dextrose Injection or a clinically appropriate electrolyte solution.*
Logo (Man03 0000 03)
Package Label (PRINCIPAL DISPLAY)
Label for Mannitol Injection, USP 25% (250 mg/mL) with a strength of 12.5 g per 50 mL in a single dose vial. The product is for intravenous use and urologic irrigation, labeled by Fresenius Kabi USA, LLC. The label includes usage instructions, storage conditions, and the NDC code 63323-024-01.*
Package Label (PRINCIPAL DISPLAY)
Label for Mannitol Injection, USP 25% (12.5 g per 50 mL, 250 mg/mL) by Fresenius Kabi USA, LLC. The product is packaged as 25 single dose vials of 50 mL each, labeled for intravenous use and urologic irrigation. The label includes storage instructions, ingredients, and manufacturer contact information.*
* 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.
