Albutein Injection, Solution
Product Images NDC 68516-5216

3 FDA label images from Grifols Usa, Llc · 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 Albutein (NDC 68516-5216). 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

Figures 1,2,3,4 (Fig 1 2 3 4)

Figures 1,2,3,4 (Fig 1 2 3 4)
An instructional diagram illustrating four steps for preparing an intravenous solution bag: Figure 1 shows hands removing a protective cap; Figure 2 depicts opening a port or spout; Figure 3 shows holding a tap or valve below the bag; and Figure 4 illustrates connecting a syringe to the bag's port for withdrawal or injection.*
FDA Label Image

Carton Label (3063683cartonalb Flexbag25 100ml)

Carton Label (3063683cartonalb Flexbag25 100ml)
Packaging label for ALBUTEIN Albutein FlexBag 25% (Albumin (Human) U.S.P.) injection solution, 25 g/100 mL strength. Label indicates 5 x 100 mL single-dose containers with storage instructions and manufacturer Grifols USA, LLC. The label design includes product name, concentration, lot and expiration details, and usage precautions.*
FDA Label Image

Bag Label (Label100)

Bag Label (Label100)
Label of ALBUTEIN FlexBag 25%, albumin (human) injection solution, 25 g/100 mL strength. The label includes details on contents, usage, storage instructions, and manufacturer GRIFOLS USA LLC. The bag features a port at the bottom for intravenous administration and displays NDC 68516-5216-8 along with barcode and QR code.*

* 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.