Potassium Chloride In Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 0338-0803

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Potassium Chloride In Dextrose And Sodium Chloride (NDC 0338-0803). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Company, 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

Image Of D-glucose Monohydrate Structural Formula (Image 01)

Chemical structure of D-Glucose monohydrate, a component of Potassium Chloride in Dextrose and Sodium Chloride injection solution.*

FDA Label Image

Representative Container Label Ndc 0338-0663-04 (Image 02)

Label for Potassium Chloride 20 mEq Injection in 5% Dextrose and 0.2% Sodium Chloride, 1000 mL intravenous solution. The label includes concentration details, volume, and manufacturer information from Baxter Healthcare Company, Deerfield, IL. It lists excipients, storage instructions, and cautions in small black text below the main product name in large red font.*

FDA Label Image

Representative Container Label 0338-0603-03 (Image 03)

Label for Potassium Chloride in Dextrose and Sodium Chloride injection, USP, containing 20 mEq potassium chloride in 5% dextrose and 0.2% sodium chloride. The label indicates a VIAFLEX Plus container with placeholders for the expiration date, lot number, and bar codes, along with container volume of 1000 mL.*

FDA Label Image

Representative Container Label Ndc 0338-0669-04 (Image 04)

Potassium Chloride 10 mEq in 5% Dextrose and 0.33% Sodium Chloride Injection USP, 500 mL vial label. The label shows dosage details, pH range, osmolarity, and storage instructions. Manufactured by Baxter Healthcare Corporation, Deerfield, IL, USA.*

FDA Label Image

Representative Container Label Ndc 0338-0671-03 (Image 05)

Packaging label for Potassium Chloride in Dextrose and Sodium Chloride injection, USP, showing a container size of 24-500 mL. The label includes dosage information: 10 mEq Potassium Chloride in 5% Dextrose and 0.33% Sodium Chloride. It displays placeholders for expiration date, lot number, and corresponding primary and secondary bar codes. Labeler is Baxter Healthcare Company.*

FDA Label Image

Representative Container Label 0338-0673-04 (Image 06)

Potassium Chloride in Dextrose and Sodium Chloride Injection, Solution in a 1000 mL plastic container. The label shows 10 mEq Potassium Chloride strength, with 5 g Dextrose and 0.45% Sodium Chloride per liter. The solution pH is 4.5, labeled for intravenous use. Manufactured by Baxter Healthcare Company, Deerfield, IL, USA.*

FDA Label Image

Representative Container Label Ndc 0338-0675-04 (Image 07)

Label for Potassium Chloride in Dextrose and Sodium Chloride injection in a VIAFLEX Plus container, containing 10 mEq potassium chloride in 5% dextrose and 0.45% sodium chloride. The label includes fields for expiration date, lot number, and two barcodes (primary and secondary). The container volume is 1000 mL.*

FDA Label Image

Representative Container Label Ndc 0338-0803-04 (Image 08)

Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection USP in a 500 mL VIAFLEX Plus container. The label shows the active ingredients Potassium Chloride (10 mEq), Dextrose Hydrous (5 g per 100 mL), and Sodium Chloride (450 mg per 100 mL). Manufactured and labeled by Baxter Healthcare Corporation, Deerfield, IL, USA.*

FDA Label Image

Representative Container Label Ndc 0338-0807-04 (Image 09)

Label for Potassium Chloride in Dextrose and Sodium Chloride injection, solution in VIAFLEX Plus container. It specifies 10 mEq Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride, USP, with a volume of 500 mL. Includes placeholders for expiration date, lot number, and barcode information.*

* 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.