Dextrose And Electrolyte No. 48 Injection
Product Images NDC 0338-0143

3 FDA label images from Baxter Healthcare Company · 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 Dextrose And Electrolyte No. 48 (NDC 0338-0143). 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Image 01)

Structural Formula (Image 01)
Chemical structure of d-Glucopyranose monohydrate, depicting the molecular arrangement with hydroxyl groups, carbon atoms, and a water molecule (H2O). The structure shows a cyclic form of glucose with a CH2OH group and various hydroxyl substitutions.*
FDA Label Image

5% Dextrose And Electrolyte Representative Container Label (Image 02)

5% Dextrose And Electrolyte Representative Container Label (Image 02)
Label of 5% Dextrose and Electrolyte No. 48 Injection, a 500 mL intravenous solution containing multiple electrolytes and dextrose. The label lists ingredient quantities per 100 mL and includes storage instructions and usage cautions. The product is by Baxter Healthcare Company, Deerfield, IL, USA, with NDC 0338-0143.*
FDA Label Image

5% Dextrose And Electrolyte Representative Carton Label (Image 03)

5% Dextrose And Electrolyte Representative Carton Label (Image 03)
Label for Dextrose and Electrolyte No. 48 Injection 5% in a 500 mL Viaflex container by Baxter Healthcare Company. The label includes space for secondary and primary bar codes, expiration date, and lot number, along with the product name and concentration details.*

* 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.