Dextrose Injection, Solution
Product Images NDC 0990-7935

11 FDA label images from Icu Medical Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 0990-7935). 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 For Dextrose Injection, Usp (Dextrose 01)

Structural Formula For Dextrose Injection, Usp (Dextrose 01)
Chemical structure of dextrose monohydrate, showing the cyclic form of the sugar molecule with hydroxyl groups and an attached water molecule (H2O).*
FDA Label Image

Pprincipal Display Panel (70 g/100 mL Bag Label)

Pprincipal Display Panel (70 g/100 mL Bag Label)
Dextrose Injection, USP 70% solution in a 1000 mL partial-fill container. The label shows each 100 mL contains 70 g dextrose in water for injection, specifies hypertonic osmolality, specific gravity 1.236, and pH range 3.2 to 6.5. It includes cautions for administration only after dilution, sterility, single dose use, and storage instructions. Labeler is ICU Medical Inc.*
FDA Label Image

Principal Display Panel (70 g/100 mL Bag Overwrap)

Principal Display Panel (70 g/100 mL Bag Overwrap)
This text panel provides handling and storage instructions for an intravenous dextrose injection solution. It advises tearing at the notch to open, inspecting the moisture and oxygen barrier overwrap for damage, and discarding if compromised. Instructions include temperature storage conditions (20 to 25°C), protecting from freezing, and checking the container for leaks after removing the overwrap. Contains the manufacturer ICU Medical Inc. details and barcode above the instructions.*
FDA Label Image

Principal Display Panel (20 g/100 mL Bag Label)

Principal Display Panel (20 g/100 mL Bag Label)
Label of Dextrose 20% Injection, USP, 500 mL partial-fill container for intravenous use. The label states each 100 mL contains 20 grams of dextrose in water for injection. Manufacturer is ICU Medical Inc. The label includes dosing cautions, pH range (4.3 to 6.5), and storage instructions. It also notes the solution is hypertonic, single-dose, sterile, and nonpyrogenic.*
FDA Label Image

Principal Display Panel (20 g/100 mL Bag Overwrap)

Principal Display Panel (20 g/100 mL Bag Overwrap)
A text panel for Dextrose injection solution by ICU Medical Inc. It provides storage and handling instructions, emphasizing the moisture and oxygen barrier overwrap, checking for tears or holes, proper storage temperature (20 to 25°C or 68 to 77°F), protection from freezing, and leak inspection before use. The panel also notes this is Rx only.*
FDA Label Image

Principal Display Panel (50 g/100 mL Bag Label)

Principal Display Panel (50 g/100 mL Bag Label)
Dextrose 50% Injection, USP solution in a 500 mL intravenous partial-fill container by ICU Medical Inc. The label states each 100 mL contains 50 g dextrose in water for injection with hypertonic osmolarity. It includes cautions for dilution and administration, instructions for storage, and warnings about sterility and additives.*
FDA Label Image

Principal Display Panel (50 g/100 mL Bag Overwrap)

Principal Display Panel (50 g/100 mL Bag Overwrap)
This text panel provides handling and storage instructions for a sterile intravenous dextrose injection solution. It advises to tear at the notch to open, keep the unit in its moisture and oxygen barrier overwrap until use, inspect for damage, store at 20 to 25°C (68 to 77°F), protect from freezing, and check for leaks before use. The labeler is ICU Medical, Inc., Lake Forest, Illinois.*
FDA Label Image

Principal Display Panel (40 g/100 mL Bag Label)

Principal Display Panel (40 g/100 mL Bag Label)
40% Dextrose Injection, USP in a 500 mL intravenous solution container by ICU Medical Inc. The label states each 100 mL contains 40 g of dextrose, hydrous. It includes cautionary information about administration only after dilution via central venous catheter and incompatibility warnings. The label notes it is a single-dose, sterile, nonpyrogenic container for intravenous use with a pH of 4.3 (range 3.2 to 6.5).*
FDA Label Image

Principal Display Panel (40 g/100 mL Bag Overwrap)

Principal Display Panel (40 g/100 mL Bag Overwrap)
This text panel provides handling and storage instructions for Dextrose injection solution by ICU Medical Inc. It advises to tear at notch to open, inspect the moisture and oxygen barrier overwrap for damage, store at 20 to 25°C (68 to 77°F), protect from freezing, and check for leaks after removing the overwrap. Contains manufacturer details and a barcode.*
FDA Label Image

Principal Display Panel (30 g/100 mL Bag Label)

Principal Display Panel (30 g/100 mL Bag Label)
Label for Dextrose Injection, USP 30% strength in a 500 mL partial-fill container. The label states it contains 30 g dextrose hydrous per 100 mL in water for injection, with pH 4.3 (range 3.2 to 6.5), and a calculated osmolarity of 1514 mOsmol/L. It includes safety cautions about hypertonic solution administration and additive incompatibility. The label also notes single-dose use for intravenous injection only, marked Rx only, and lists ICU Medical, Inc. as the labeler.*
FDA Label Image

Principal Display Panel (30 g/100 mL Bag Overwrap)

Principal Display Panel (30 g/100 mL Bag Overwrap)
A drug information panel for Dextrose injection, solution from ICU Medical Inc. It provides instructions for opening and handling the overwrap, storage temperature (20 to 25°C), protection from freezing, and guidance to check for leaks before use, with disposal instructions if sterility is compromised.*

* 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.