Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 63323-874

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 63323-874). 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.

FDA Label Image

Structural Formula (Dex0x 0001 01)

Structural Formula (Dex0x 0001 01)
D-Glucose monohydrate is a type of glucose that contains one molecule of water in its chemical structure. Glucose is a simple sugar that is an important source of energy for the body's cells. It is commonly found in fruits, vegetables, and honey, and is often used as a sweetener in food products. D-Glucose monohydrate is widely used in the pharmaceutical industry and in the production of various chemicals.*
FDA Label Image

Logo (Dex0x 0001 02)

FDA Label Image

Package Label (PRINCIPAL DISPLAY –2.5% Dextrose and 0.45% Sodium)

Package Label (PRINCIPAL DISPLAY –2.5% Dextrose and 0.45% Sodium)
This is a description of a medication product called "freeflex" that is presented in a 1000-milliliter container. The medication contains 2.5% dextrose and 0.45% sodium chloride, and it's designed to be used intravenously. This medication does not contain natural rubber latex; it's sterile, and the container is made of Non-PVC, Non-DEHP material. It's recommended to store the medication at a temperature between 68 and 77 degrees Fahrenheit (20 ℃ to 25 ℃). The dosage is specified in the package insert, and the medication should be used immediately upon removal of the moisture barrier overwrap. The text also provides specific details about the composition of the medication, including the electrolytes present.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – 2.5% Dextrose and 0.45%)

Package Label (PRINCIPAL DISPLAY – 2.5% Dextrose and 0.45%)
This is a prescription-only solution for injection that contains 2.5% dextrose and 0.45% sodium chloride. The NDC code is 63323-874-10, and it comes in a pack of ten 1000 mL single-dose flexible containers. It is manufactured for Fresenius Kabi USA LLC and should be stored at 20° to 25°C until ready to use to avoid excessive heat. The lot number and expiration date are provided, and the solution is made in Germany.*

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