Human Albumin Grifols Solution
Product Images NDC 61953-0001

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Human Albumin Grifols (NDC 61953-0001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Grifols Usa, Llc, 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

61953 0001 3 Label

Label for HUMAN ALBUMIN GRIFOLS 20% solution containing 10 g/50 mL of ALBUMIN (HUMAN) for intravenous use. The label includes storage instructions, manufacturer information (Instituto Grifols, S.A., Barcelona, Spain), and barcode. It is marked Rx only and shows the GRIFOLS brand logo with product identifiers and handling instructions.*

FDA Label Image

61953 0001 4 Label

Label for HUMAN ALBUMIN GRIFOLS 20% solution, 100 mL intravenous dosage form. The label includes product content details, storage instructions, manufacturer Instituto Grifols, S.A. in Barcelona, Spain, and U.S. license information. It also features a barcode, lot number, and expiration date fields.*

FDA Label Image

Carton 61953 0001 1

Packaging label for HUMAN ALBUMIN GRIFOLS 10 g/50 mL solution, an intravenous plasma derivative containing 20% Albumin (Human) by Grifols USA, LLC. The label includes storage instructions, precautions for use, and manufacturing information from Instituto Grifols, S.A., Barcelona, Spain. NDC 61953-0001.*

FDA Label Image

Carton 61953 0001 2

The packaging label for HUMAN ALBUMIN GRIFOLS 20% solution, 20 g/100 mL, an intravenous plasma derivative by Grifols USA, LLC. The label includes dosing instructions, storage conditions, product contents, and manufacturer details from Instituto Grifols, S.A., Spain. It features multiple barcodes and prominent brand name branding on a blue and white background.*

* 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.