Dextrose And Sodium Chloride Injection, Solution
Product Images NDC 0338-0077

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Dextrose And Sodium Chloride (NDC 0338-0077). 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

Chemical Structure (Image 01)

Chemical Structure (Image 01)
Chemical structure of D-Glucose monohydrate, shown as part of the active ingredients related to Dextrose and Sodium Chloride injection solution by Baxter Healthcare Company.*
FDA Label Image

Dextrose And Sodium Chloride Representative Container Label Ndc 0338-0089-03 (Image 02)

Dextrose And Sodium Chloride Representative Container Label Ndc 0338-0089-03 (Image 02)
Label for 5% Dextrose and 0.9% Sodium Chloride Injection USP in a 500 mL intravenous solution. The label includes details on concentrations, pH, osmolarity, storage conditions, and cautions. It is a sterile, nonpyrogenic single-dose container from Baxter Healthcare Corporation, Deerfield, IL, USA.*
FDA Label Image

Dextrose & Sodium Chloride Representatve Carton Label Ndc 0338-0089-036 (Image 03)

Dextrose & Sodium Chloride Representatve Carton Label Ndc 0338-0089-036 (Image 03)
Label for Dextrose and Sodium Chloride injection solution, USP, containing 5% dextrose and 0.9% sodium chloride. The label specifies a 500 mL VIAFLEX container with placeholders for expiration date, lot number, a secondary barcode, and a primary barcode. The product is labeled by Baxter Healthcare Company.*
FDA Label Image

Dextrose & Sodium Chloride Representative Container Label Ndc 0338-0073-04 (Image 04)

Dextrose & Sodium Chloride Representative Container Label Ndc  0338-0073-04 (Image 04)
Label for Dextrose and Sodium Chloride Injection USP, 2.5% Dextrose and 0.45% Sodium Chloride solution, 1000 mL intravenous injection. The label includes concentration details, pH, osmolarity, storage instructions, and manufacturer information. The product is made by Baxter Healthcare Corporation, Deerfield, IL, USA, and the container type is Viaflex PL 146 plastic.*
FDA Label Image

Dextrose & Sodium Chloride Representative Carton Label Ndc 0338-0073-042 (Image 05)

Dextrose & Sodium Chloride Representative Carton Label Ndc 0338-0073-042 (Image 05)
Label for Dextrose and Sodium Chloride injection, solution, 2.5% dextrose and 0.45% sodium chloride, in a 1000 mL Viaflex container. The label shows space for expiration date, lot number, primary and secondary bar codes. The product is by Baxter Healthcare Company.*
FDA Label Image

Dextrose & Sodium Chloride Representative Container Label Ndc 0338-0077-02 (Image 06)

Dextrose & Sodium Chloride Representative Container Label Ndc 0338-0077-02 (Image 06)
Label for 5% Dextrose and 0.2% Sodium Chloride Injection USP, 250 mL vial. The label includes dosing and storage instructions, sterility cautions, and manufacturer information. The product is distributed by Baxter Healthcare Corporation, Deerfield, IL, USA, with contact information and a lot and expiration date section.*
FDA Label Image

Dextrose And Sodium Chloride Representative Carton Label 0338-0077-02 (Image 07)

Dextrose And Sodium Chloride Representative Carton Label 0338-0077-02 (Image 07)
A text panel showing product identification and barcode information for 5% Dextrose and 0.2% Sodium Chloride Injection, USP in a VIAFLEX® container. It includes placeholders for expiration date, lot number, and primary and secondary bar codes specific to this intravenous solution by Baxter Healthcare Company.*
FDA Label Image

Dextrose And Sodium Chloride Representative Container Label 0338-0081-03 (Image 08)

Dextrose And Sodium Chloride Representative Container Label 0338-0081-03 (Image 08)
Label for 5% Dextrose and 0.33% Sodium Chloride Injection USP, 500 mL solution for intravenous use. The label includes detailed ingredient concentrations, pH range, sterility information, storage instructions, and manufacturer details for Baxter Healthcare Corporation, Deerfield, IL, USA.*
FDA Label Image

Dextrose And Sodium Chloride Representative Carton Label 0338-0081-03 (Image 09)

Dextrose And Sodium Chloride Representative Carton Label 0338-0081-03 (Image 09)
Label of a 500 mL VIAFLEX container of Dextrose and Sodium Chloride injection, USP, showing 5% dextrose and 0.33% sodium chloride solution. The label includes placeholders for expiration date, lot number, and bar codes, with the primary bar code number displayed.*
FDA Label Image

Dextrose & Sodium Chloride Representative Container Label Ndc 0338-0085-03 (Image 10)

Dextrose & Sodium Chloride Representative Container Label Ndc 0338-0085-03 (Image 10)
Label of 5% Dextrose and 0.45% Sodium Chloride Injection USP, 500 mL solution for intravenous use. The label includes concentration details, pH, osmolarity, administration instructions, storage conditions, lot and expiration placeholders, Baxter Healthcare Company as the labeler, and contact information. Container type is VIAFLEX plastic.*
FDA Label Image

Dextrose & Sodium Chloride Representative Carton Label Ndc 0338-0085-038 (Image 11)

Dextrose & Sodium Chloride Representative Carton Label Ndc 0338-0085-038 (Image 11)
Label for Dextrose and Sodium Chloride Injection, USP, 5% Dextrose and 0.45% Sodium Chloride, in a 500 mL Viaflex container. The label includes placeholders for expiration date, lot number, secondary and primary bar codes, and a GTIN number beneath the primary bar code.*

* 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.