Jynneos Injection, Powder, Lyophilized, For Suspension
Product Images NDC 50632-024

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Jynneos (NDC 50632-024). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bavarian Nordic A/s, 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

Reconstitution Instructions (Image 01)

Illustration showing the preparation steps for JYNNEOS vaccine injection. The sequence depicts withdrawing diluent from vial B and transferring it into vial A containing the lyophilized antigen, gently shaking vial A until the powder dissolves, and finally withdrawing 0.5 mL of the reconstituted vaccine from vial A for subcutaneous administration.*

FDA Label Image

Jynneos Lyophilized Antigen Component Carton Label (Image 02)

Packaging label for JYNNEOS Smallpox and Mpox Vaccine, Live, Non-replicating, lyophilized antigen component for injection. The label specifies the product as a lyophilized antigen component that must be combined with a sterile water diluent to form a single 0.5 mL dose. It is manufactured by Bavarian Nordic A/S and requires refrigeration. The label emphasizes it is not to be used alone and is for subcutaneous use only.*

FDA Label Image

Lyophilized Antigen Component Vial Label (Image 03)

Label for JYNNEOS vaccine, containing lyophilized antigen component for injection, 0.5 mL dose. The label states it is not to be used alone and must be reconstituted with diluent to form the final vaccine. Manufacturer is Bavarian Nordic A/S. Includes NDC 50632-024-04, lot number, and expiration date fields along with barcodes.*

* 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.