Dextrose Injection, Solution
Product Images NDC 65219-238

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 65219-238). 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

Dex11 0004 01

FDA Label Image

Dex11 0004 02

Chemical structure of Dextrose Monohydrate showing its molecular ring form with hydroxyl groups and a water molecule (H2O) attached, consistent with the monohydrate form.*

FDA Label Image

Dex11 0004 03

FDA Label Image

Dex11 0004 04

Label for 5% Dextrose Injection, USP containing 2.5 grams per 50 mL (50 mg/mL) of dextrose monohydrate in an intravenous injection solution. The label includes usage instructions, storage conditions (20° to 25°C), and manufacturer details for Fresenius Kabi USA, LLC, made in Norway. It features a barcode and safety information such as single dose use and latex-free container closure.*

FDA Label Image

Dex11 0004 05

Label for 5% Dextrose Injection, USP, freeflex+ format, 50 mL vial, pack of 60, manufactured by Fresenius Kabi USA, LLC. Storage instructions are 20° to 25°C (68° to 77°F), protect from freezing. Made in Norway. Includes barcode, lot, and expiration placeholders.*

FDA Label Image

Dex11 0004 06

Label for 5% Dextrose Injection, USP, 5 grams per 100 mL (50 mg per mL) intravenous solution. The product contains dextrose monohydrate and water for injection. Manufactured for Fresenius Kabi USA, LLC, Lake Zurich, IL. The label includes storage instructions, use guidelines, barcoding, and manufacturing details, noting the container is non-PVC, sterile, and made without natural rubber latex. Made in Norway.*

FDA Label Image

Dex11 0004 07

Label for 5% Dextrose Injection, USP, 100 mL, packaged in a quantity of 50 units. The product is manufactured by Fresenius Kabi USA, LLC, with manufacturing location in Norway. Storage instructions note to keep at 20° to 25°C and protect from freezing. The label features barcodes, expiration and lot number placeholders, and the Fresenius Kabi logo.*

FDA Label Image

Dex11 0004 08

Label for 5% Dextrose Injection, USP, 12.5 grams per 250 mL (50 mg per mL) intravenous solution by Fresenius Kabi USA, LLC. The label includes NDC 65219-238-01 and details such as composition per 100 mL (5 g dextrose monohydrate, 100 mL water for injection), pH, storage instructions at 20° to 25°C, and single-dose use. The container is sterile, non-PVC, non-DEHP, and latex-free. Manufacturer location is Lake Zurich, IL, with product made in Germany.*

FDA Label Image

Dex11 0004 09

Label for 5% Dextrose Injection, USP, 250 mL vial, pack of 30. The label displays the brand freeflex and includes storage instructions to keep at 20° to 25°C, protecting from freezing. Manufactured for Fresenius Kabi USA, LLC, with manufacturing location noted as Germany. The label includes a barcode and space for lot and expiration dates.*

FDA Label Image

Dex11 0004 10

Label for 5% Dextrose Injection, USP, 25 grams per 500 mL (50 mg/mL) intravenous solution by Fresenius Kabi USA, LLC. Contains dextrose monohydrate and water for injection. The label includes storage instructions, usage precautions, a barcode, and manufacturing information stating it is made in Germany.*

FDA Label Image

Dex11 0004 11

Label for 5% Dextrose Injection, USP, 500 mL solution for intravenous injection by Fresenius Kabi USA, LLC. The label indicates storage instructions and includes a barcode, lot, and expiration date fields, with product and manufacturer details, including manufacturing in Germany.*

* 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.