Formula1.jpg (Formula1)
Chemical structure of Mannitol showing a six-carbon chain with hydroxyl groups (OH) attached, representing its molecular structure.*
Mannitol Injection, Solution
Product Images NDC 0404-9905
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 Mannitol (NDC 0404-9905). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Henry Schein, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Image1.jpg (Image1)
A table listing adverse reactions associated with Mannitol injection, solution 12.5 g/50mL by Henry Schein, Inc. It categorizes reactions by system including hypersensitivity, renal failure, CNS toxicity, fluid and electrolyte imbalances, infusion site reactions, cardiac and respiratory disorders, gastrointestinal disorders, and general disorders, with specific symptoms for each category.*
Image2.jpg (Image2)
A data table showing solution concentration information for Mannitol injection. It lists concentration as 25%, 25 grams per 100 mL, measured osmolality at 1372 mOsmol/liter, and a pH range of 4.5 to 7.0. A note mentions possible pH adjustments with sodium bicarbonate and/or hydrochloric acid.*
Label1.jpg (Label1)
Label for Mannitol 12.5 g/50 mL injection, USP, 25% solution in a single dose fliptop vial. The label includes usage instructions, warnings for intravenous use only, storage conditions (20 to 25°C), and packaging by Henry Schein, Inc., Bastian, VA. The National Drug Code (NDC) number 0404-9905-50 is also printed.*
* 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.
