Ionosol Mb And Dextrose Injection, Solution
Product Images NDC 0990-7372

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ionosol Mb And Dextrose (NDC 0990-7372). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Icu Medical 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.

FDA Label Image

Structural Formula Dextrose (Ionosol 01)

Chemical structure diagram of Dextrose Monohydrate showing the molecular arrangement with hydroxyl groups and a water molecule (H2O).*

FDA Label Image

Principal Display Panel (500 mL Bag Label)

Label for Ionosol MB and Dextrose 5% Dextrose Injection, a maintenance electrolyte solution injection. It contains dextrose monohydrate 5 g, magnesium chloride hexahydrate 30 mg, potassium chloride 141 mg, monobasic potassium phosphate anhydrous 15 mg, monobasic sodium phosphate monohydrate 25 mg, and sodium lactate anhydrous 260 mg per 100 mL. The label notes electrolyte concentrations per liter, pH range 4.0 to 6.5, and instructions about additive incompatibility and aseptic technique. The product is labeled for intravenous use, single-dose container, and manufactured for ICU Medical Inc.*

FDA Label Image

Principal Display Panel (Overwrap Label)

A text panel providing opening instructions and storage information for a drug product. It advises tearing at the notch to open, checking for leaks by squeezing the container, and discarding if leaks are found. It recommends storage at room temperature (25°C), avoiding excessive heat, and protecting from freezing.*

* 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.