Cardioplegic Solution
Product Images NDC 0338-0341

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 Cardioplegic (NDC 0338-0341). 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

Cardioplegic Solution Representative Container Label (Image 01)

Cardioplegic Solution Representative Container Label (Image 01)
Cardioplegic Solution label for intra-arterial use by Baxter Healthcare Corporation. The solution contains Calcium Chloride 17.6 mg/100mL, Magnesium Chloride 325.3 mg/100mL, Potassium Chloride 119.3 mg/100mL, and Sodium Chloride 643 mg/100mL. The 1000 mL flexible container warns against intravenous injection and instructs aseptic technique. The label includes a precaution to add 10 mL of 8.4% Sodium Bicarbonate Injection before use and storage guidelines. The product NDC is 0338-0341-04.*
FDA Label Image

Representative Cardioplegic Solution Carton Label Panel 1 (Image 02)

Representative Cardioplegic Solution Carton Label Panel 1 (Image 02)
Cardioplegic Solution label for Baxter Healthcare Corporation, presented in a Viaflex container with a volume of 1000 mL. The label includes large text with the product name and container size, placeholders for bar codes, expiration date, and lot number, and instructions to protect the solution from freezing.*
FDA Label Image

Representative Cartioplegic Solution Carton Label Panel 2 (Image 03)

Representative Cartioplegic Solution Carton Label Panel 2 (Image 03)
Label for Cardioplegic Solution, displaying the product name prominently along with a lot number (2B1462X). It specifies a 1000 mL Viaflex container and advises protection from freezing. An expiration date placeholder is shown as YYYY-MM-DD. The label does not show strength 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.