Diluent Injection
Product Images NDC 49281-912

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diluent (NDC 49281-912). 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

Principal Display Panel (0.5 mL Vial Label)

Label for YF-VAX Yellow Fever Vaccine 4.5 mg/.5 mL single-dose injection, lyophilized for suspension. The label shows the NDC 49281-915-58, indicates it is Rx only, and lists Sanofi Pasteur Inc. as manufacturer. Space is reserved for lot, expiration, and a 2D barcode information.*

FDA Label Image

Principal Display Panel (5 Vial Package)

Packaging label for Yellow Fever Vaccine YF-VAX by Sanofi Pasteur. The label specifies the vaccine as a live 17D virus, freeze-dried, avian leukosis-free, sorbitol-gelatin stabilized. It indicates supply in 5 single-dose vials, with storage instructions to keep between 2° to 8°C and not to freeze. The label includes directions for reconstitution with 0.6 mL diluent and subcutaneous administration of 0.5 mL dose.*

FDA Label Image

Principal Display Panel (0.6 mL Vial Label)

Label for Sodium Chloride Injection USP, single-dose 0.6 mL, for reconstitution of 1 dose Yellow Fever Vaccine only. Manufactured by Sanofi Pasteur Inc., Swiftwater PA 18370 USA. Includes an NDC barcode and note indicating location of lot, expiration, and 2D barcode.*

FDA Label Image

Principal Display Panel (5 Vial Package)

Packaging label for Sodium Chloride Injection USP, a diluent for single-dose Yellow Fever Vaccine. The label shows a 5 single-dose vial carton (0.6 mL each) manufactured by Sanofi Pasteur. It includes storage instructions advising not to freeze and to discard within 8 hours after opening. Sodium Chloride concentration is 0.9% with total osmolarity of 286 milliosmoles per liter.*

* 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.