Kedbumin Injection, Solution
Product Images NDC 76179-025

2 FDA label images from Kedrion S.p.a · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Kedbumin (NDC 76179-025). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kedrion S.p.a, 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

Package Label – Principal Display Panel – 50 mL Vial (Kedbumin 01)

Package Label – Principal Display Panel – 50 mL Vial (Kedbumin 01)
Label for KEDBUMIN 25% injection, solution containing 12.5 g/50 mL Albumin (Human), a plasma derivative for intravenous use. The label includes storage instructions to protect from light and maintain temperature below 30°C, caution for not using if solution is turbid, and a note to administer within 4 hours after vial entry. Distributed by Kedrion Biopharma in Fort Lee, NJ, and manufactured by Kedrion S.p.A in Italy. Contains warnings, contents, lot and expiration date fields, and barcode.*
FDA Label Image

Package Label – Principal Display Panel – 50 mL Carton (Kedbumin 02)

Package Label – Principal Display Panel – 50 mL Carton (Kedbumin 02)
Packaging label for KEDBUMIN 25%, containing Albumin (Human) U.S.P. Injection, Solution 12.5 g per 50 mL vial. The label includes storage instructions, lot and expiration date placeholders, cautions for intravenous infusion only, and manufacturer information. It is labeled by Kedrion S.p.A and distributed by Kedrion Biopharma, Inc. The label prominently features '25%' and the product's barcode.*

* 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.