Imovax Rabies Kit
Product Images NDC 49281-252

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Imovax Rabies (NDC 49281-252). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sanofi Vaccines Us Inc., 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 (Imovax 01)

An instructional diagram showing a syringe with labeled parts, including the plunger rod, syringe barrel, syringe cap, and tip cap, with an arrow indicating the removal direction of the tip cap.*

FDA Label Image

Figure (Imovax 02)

An instructional illustration showing hands holding a syringe-like device. One hand is stabilizing the syringe while the other hand is gripping the cap, with an arrow indicating a twisting motion to remove or open the cap. The image demonstrates a step in preparing or accessing the contents of the device.*

FDA Label Image

Figure (Imovax 03)

An instructional illustration showing hands assembling or connecting two components of a syringe or injection device. One hand holds a syringe while the other hand holds a separate piece, demonstrating a twisting or locking motion indicated by an arrow. This diagram likely depicts part of the preparation or use process for the vaccine kit.*

FDA Label Image

Principal Display Panel (1 mL Vial Label)

Label for IMOVAX RABIES rabies vaccine single-dose vial, 1 mL. It indicates the vaccine is for intramuscular (IM) use only and is manufactured by Sanofi Pasteur SA in Lyon, France, distributed by Sanofi Pasteur Inc. in Swiftwater, PA, USA. The label includes a barcode and references US government license #1724.*

FDA Label Image

Principal Display Panel (1 mL Syringe Label)

Label for sterile water diluent for reconstitution, single-dose 1 mL vial. The label states USP standards, contains no preservative, and is intended for Rx only. The label includes the NDC 49281-263-58 and the manufacturer Sanofi Pasteur.*

FDA Label Image

Principal Display Panel (Kit Carton)

IMOVAX RABIES vaccine kit for human use, single-dose 1 mL vial, manufactured by Sanofi Pasteur SA, Lyon France, and distributed by Sanofi Pasteur Inc. The label indicates the vaccine is a rabies vaccine for intramuscular injection only, with potency equal to or greater than 2.5 IU/mL of rabies antigen. The packaging includes barcode, lot and serial number area, storage instructions (2°C to 8°C), and warnings against intradermal use.*

FDA Label Image

Principal Display Panel (1 mL Vial Label)

IMOVAX RABIES vaccine label for a 1 mL dose, indicated for intramuscular (IM) and rabies (R) use only. The label includes the product name, manufacturer Sanofi Pasteur SA in Lyon, France, distributor Sanofi Pasteur Inc. in Swiftwater, PA, barcode, NDC 49281-248-58, and US government license number 1724.*

FDA Label Image

Principal Display Panel (1 mL Syringe Label)

Label for sterile water diluent for reconstitution, USP, supplied in a 1 mL volume. The label indicates it contains no preservative and is for prescription use only. The product is manufactured by Sanofi Pasteur and includes an NDC barcode and number 49281-249-01.*

FDA Label Image

Principal Display Panel (Kit Carton)

IMOVAX RABIES kit packaging label for Rabies Virus Strain PM-1503-3M antigen vaccine. The label includes the proprietary name IMOVAX RABIES, indicates it is a rabies vaccine for intramuscular injection only, with 1 dose (1 mL) per kit. Manufactured by Sanofi Pasteur SA and distributed by Sanofi Pasteur Inc. The label includes storage instructions, product NDC 49281-250-51, and a barcode.*

* 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.