Plegisol Injection, Solution
Product Images NDC 0409-7969

4 FDA label images from Hospira, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Plegisol (NDC 0409-7969). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, Inc., 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

Logo (Plegisol 01)

FDA Label Image

Iv Bag Ndc 0409-7969-05 (Plegisol 02)

Iv Bag Ndc 0409-7969-05 (Plegisol 02)
This image shows a caution label panel instructing the use of aseptic technique and the requirement to add 10 mL of 8.4% Sodium Bicarbonate Injection prior to use. It advises on packaging opening, checking for leaks, storage temperature (20°C to 25°C / 68°F to 77°F), and protection from freezing. It states the product is not made with natural rubber latex.*
FDA Label Image

Principal Display Panel (Pouch Label)

Principal Display Panel (Pouch Label)
Plegisol injection solution label from Hospira, Inc. for intra-arterial administration. The label states it is Hospira's cardioplegic solution for cardiac perfusion, with warnings against intravenous injection. It lists active ingredients: sodium chloride 643 mg, calcium chloride 17.6 mg, magnesium chloride 325.3 mg, and potassium chloride 119.3 mg per 100 mL. The label includes instructions for pH adjustment and storage, identifies the solution as sterile and nonpyrogenic, and features the product NDC 0409-7969-11.*
FDA Label Image

Plegisol 04

Plegisol 04
Label for Plegisol injection, solution, a single-dose 1000 mL container. It is Hospira Inc's cardioplegic solution with electrolytes including sodium, potassium, magnesium, calcium, chloride, and bicarbonate. The label warns it is not for intravenous injection and provides storage and handling instructions. NDC 0409-7969-11 is shown.*

* 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.