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)

This is a vaccine called Yellow Fever manufactured by Sanofi Pasteur Inc. with the brand name YF-VAX. The product has a specific NDC number, which is 49281-915-58. There is additional information related to the location of the lot, expiration, and a 2D barcode.*

FDA Label Image

Principal Display Panel (5 Vial Package)

This is information related to a Yellow Fever Vaccine with the Lot Number 2052. The text mentions the location for expiration date, serial number, and barcode. It also provides instructions for storing and administering the vaccine. The vaccine is prepared from avian leukosis-free chicken embryos infected with 17D virus and there is no preservative added. There is a dosage mentioned as well as a note to discard the unused portion. The vaccine is produced by SANOFIPASTEUR.*

FDA Label Image

Principal Display Panel (0.6 mL Vial Label)

This is a description of a medical product with the National Drug Code (NDC) number 49281-912-59. It is a reconstitution injection of Sodium Chloride for use with a single dose Yellow Fever Vaccine. The product is manufactured by Sanofi Pasteur Inc. and comes with a 2D barcode that has information about the lot number, expiration, and location.*

FDA Label Image

Principal Display Panel (5 Vial Package)

This is a description of a product, specifically an injectable diluent used for a yellow fever vaccine. The diluent comes in the form of five single-dose vials, each containing 0.6 mL of sodium chloride injection USP. The vials are labeled with a lot number, expiration date, and 2D barcode. The manufacturer of the product is Sanofi Pasteur. The text also advises against freezing the product and instructs to discard any unused portions within 8 hours of opening. The total osmolarity of the product is 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.