Imovax Rabies Kit
Product Images NDC 49281-252

3 FDA label images from Sanofi Vaccines Us Inc. · 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 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.

Product Images & Figures Index

FDA Label Image

Figure (Ba8d4e72 F452 4859 Ae6f 3644b4b0a78c 01)

Figure (Ba8d4e72 F452 4859 Ae6f 3644b4b0a78c 01)
An instructional line drawing showing two hands holding a syringe and vial. The right hand is twisting the vial cap off, indicated by a curved arrow showing the direction to turn. The image demonstrates how to remove the cap from the vial, likely as part of medication preparation steps.*
FDA Label Image

Figure (Ba8d4e72 F452 4859 Ae6f 3644b4b0a78c 02)

Figure (Ba8d4e72 F452 4859 Ae6f 3644b4b0a78c 02)
An instructional line drawing showing hands assembling two syringe components with arrows indicating the direction to connect them. This illustration demonstrates the assembly step for the IMOVAX RABIES vaccine kit syringe preparation.*
FDA Label Image

Principal Display Panel (Kit Carton)

Principal Display Panel (Kit Carton)
IMOVAX RABIES rabies vaccine kit with a single-dose 1 mL intramuscular immunization. The label shows the brand and generic names, NDC 49281-252-51, and states it is for pre- and postexposure use. Manufactured by Sanofi Winthrop Industrie and distributed by Sanofi Vaccines US Inc. Storage instructions and potency information are included.*

* 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.