Human Albumin Grifols Solution
Product Images NDC 61953-0001

View Photos of 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 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

61953 0001 3 Label
This is a description of a medical product, specifically human albumin Grifols that comes in a container with 100 grams and 50 mL. The recommended storage temperature is below 30°C, and it includes instructions on how to use and administer the product, which are provided in the package insert, provided by Institto Ritols, S.A from Spain. There is also a license number reference. The text seems to be missing some characters, but it provides useful information for those familiar with the language.*
FDA Label Image

61953 0001 4 Label

61953 0001 4 Label
This is a product description of Human Albumin Grifols® 20% 100 mL, which contains 20 grams of Albumin (Human) in an aqueous diluent, equivalent to 400 mL of plasma. The Sodium range is between 130-160 millequivalents per liter. The package insert contains dosage and administration instructions. The solution should be stored at temperatures below 30 °C; it does not contain preservatives. The product must not be used if turbid, and the container should not be used after 4 hours of opening. The given text also includes a product code and a number.*
FDA Label Image

Carton 61953 0001 1

FDA Label Image

Carton 61953 0001 2

* 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.