Ixiaro Injection, Suspension
Product Images NDC 42515-002

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ixiaro (NDC 42515-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Valneva Scotland Ltd., 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

Figure1 (Figure1)

Illustration showing preparation for administration of 0.25 mL dose from a syringe, indicating the expelling and discarding of excess volume above the 0.25 mL dose line.*

FDA Label Image

Figure2 (Figure2)

Label for IXIARO Japanese Encephalitis Vaccine, Inactivated, Adsorbed injection suspension by Valneva Scotland Ltd. The label states that each single dose syringe contains 0.5 mL. It is for intramuscular use and contains no preservatives. The label also includes storage instructions, distributor information, and a barcode. The NDC number 42515-002-01 is visible.*

FDA Label Image

Figure3 (Figure3)

Label for IXIARO Japanese Encephalitis Vaccine, Inactivated, Adsorbed injection by Valneva Scotland Ltd. The label includes the NDC number 42515-002-01, areas for lot and expiration information, and the text 'Rx only.' It also features a barcode and indicates the product is prescription-only.*

FDA Label Image

Figure4 (Figure4)

This image shows the full prescribing information for IXIARO, Japanese Encephalitis Vaccine, Inactivated, Adsorbed, 6 arb'U per 0.5 mL injection suspension by Valneva Scotland Ltd. It includes detailed text on vaccine administration, dosage, warnings, contraindications, adverse reactions, clinical pharmacology, and storage instructions. The text is densely packed with multiple sections and tables providing comprehensive drug information.*

* 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.