Corifact Kit
Product Images NDC 63833-518

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Corifact (NDC 63833-518). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Csl Behring Gmbh, 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

Figure 1 (Corifact 01)

An instructional or anatomical style line drawing showing a single cylindrical medical component with a flange at the top featuring multiple spokes radiating toward the center, resembling a hub or cap used in medical device assemblies.*

FDA Label Image

Figure 2 (Corifact 02)

An instructional illustration showing the assembly of a kit component, where a plunger or stopper is being inserted downward into a vial. This likely represents part of the preparation process for Corifact (Factor XIII Concentrate [Human]) kit by CSL Behring GmbH.*

FDA Label Image

Figure 3 (Corifact 03)

An instructional diagram showing the assembly of a medical device or kit components, featuring three parts vertically aligned with an arrow indicating the direction of assembly from top to bottom. It is likely related to the Corifact Factor XIII Concentrate (Human) kit by CSL Behring GmbH.*

FDA Label Image

Figure 4 (Corifact 04)

An instructional diagram showing a two-part kit assembly process. The top component, which resembles a vial or container with a screw-threaded bottom, is aligned vertically above the bottom vial or bottle with an arrow pointing downward, indicating attachment or insertion. This likely illustrates a step in preparing the Corifact Factor XIII Concentrate (Human) kit by CSL Behring GmbH.*

FDA Label Image

Figure 5 (Corifact 05)

An illustration showing a two-part vial or container assembly with a top and bottom component connected by a cap or clamp. Arrows indicate a twisting or rotational motion between the two parts, likely demonstrating how to open or connect the container components in the Corifact Factor XIII Concentrate (Human) kit by CSL Behring GmbH.*

FDA Label Image

Figure 6 (Corifact 06)

An instructional diagram showing how to connect two parts of a kit by aligning and twisting them together. The image depicts a top component and a bottom component being joined with a clockwise rotational arrow. No text or branding is visible in the illustration.*

FDA Label Image

Figure 7 (Corifact 07)

An instructional line drawing depicting a two-part medical device assembly with an arrow indicating a rotational movement at the base of the lower component. The illustration likely shows steps for assembly or activation of a device part, related to Corifact Factor XIII Concentrate (Human) kit by CSL Behring GmbH.*

FDA Label Image

Figure 8 (Corifact 08)

An instructional diagram showing the assembly or connection process of two cylindrical parts, with an arrow indicating a twisting or rotating motion to attach the top component onto the lower component.*

FDA Label Image

Principal Display Panel (1000-1600 IU Vial Label)

Label for Corifact Factor XIII Concentrate (Human) kit by CSL Behring GmbH. The label states it is for intravenous use only and provides storage instructions and stability information for the product. The label includes a barcode, product name, dosage form as kit, and manufacturer details.*

FDA Label Image

Principal Display Panel (Kit Carton)

Corifact Factor XIII Concentrate (Human) injectable kit by CSL Behring GmbH. The white and purple box packaging displays the proprietary name Corifact and nonproprietary name Factor XIII Concentrate (Human), indicating intravenous use only. The label includes storage instructions, manufacturer information, and cautions. The product NDC is 63833-518-02.*

* 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.