Dextrose Injection, Solution
Product Images NDC 0990-7120

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 0990-7120). 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

Dextrose Structural Formula (Dextrose 01)

FDA Label Image

Principal Display Panel (70 g Bag Label)

This is a Pharmacy Bulk Package of Dextrose Injection which must be diluted before use. Each 100 mL contains 70g Dextrose, Hydrous, USP in water for injection. It is sterile, non-pyrogenic with hypertonic osmolarity. Dosage and administration guidelines can be found in the package insert. The container should not be used if the closure is damaged or leaks are found, and the solution should be clear before use. It should be stored at 20 to 26°C (68 to 77°F), protected from freezing. The product contains no more than 25 meg/L of aluminum. It is manufactured by 1CU Medical, Inc, Lake Forest, Illinois, USA.*

FDA Label Image

Principal Display Panel (70 g Bag Overwrap Label)

This is a product label for a medical unit. It is intended to be kept in the moisture and oxygen barrier overwrap until ready for use. The user is instructed to visually inspect for damages before use and to store it in a controlled temperature environment. Any leaks found should be reported as sterility may be impaired. The dextrose injection may vary in color, but it is deemed normal and does not affect the product's efficacy. The manufacturer of the product is ICU Medical, Inc., based in Lake Forest, IL.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.