Lactated Ringers And Dextrose Injection, Solution
Product Images NDC 0338-0125

3 FDA label images from Baxter Healthcare Corporation · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lactated Ringers And Dextrose (NDC 0338-0125). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Chemical Structure (Image 01)

Chemical Structure (Image 01)
Chemical structure of Dextrose Monohydrate, showing the molecular arrangement including hydroxyl groups and associated water molecule (H2O).*
FDA Label Image

Lactated Ringer's And 5% Dextrose Injection, Usp Container Label (Image 02)

Lactated Ringer's And 5% Dextrose Injection, Usp Container Label (Image 02)
Label for Lactated Ringer's and 5% Dextrose Injection USP, 500 mL, by Baxter Healthcare Corporation. The injection solution contains 5 g dextrose hydrous, 600 mg sodium chloride, 310 mg sodium lactate, 30 mg potassium chloride, and 20 mg calcium chloride per 100 mL. The label includes storage instructions, warnings, and lot/expiration fields, with Baxter company and contact information.*
FDA Label Image

Lactated Ringer's And 5% Dextrose Injection Usp Carton Label (Image 03)

Lactated Ringer's And 5% Dextrose Injection Usp Carton Label (Image 03)
The image shows a label for Lactated Ringer's and 5% Dextrose Injection, USP in a 24-500 mL VIAFLEX container. It includes space for expiration date, lot number, secondary and primary bar codes, and the GTIN (01) 5030380125031. The label indicates use for high-resolution inkjet printing.*

* 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.