Product Images Diluent

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Product Label Images

The following 4 images provide visual information about the product associated with Diluent NDC 49281-912 by Sanofi Pasteur Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

PRINCIPAL DISPLAY PANEL - 0.5 mL Vial Label - yf vax 01

PRINCIPAL DISPLAY PANEL - 0.5 mL Vial Label - yf vax 01

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.*

PRINCIPAL DISPLAY PANEL - 5 Vial Package - yf vax 01a

PRINCIPAL DISPLAY PANEL - 5 Vial Package - yf vax 01a

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.*

PRINCIPAL DISPLAY PANEL - 0.6 mL Vial Label - yf vax 02

PRINCIPAL DISPLAY PANEL - 0.6 mL Vial Label - yf vax 02

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.*

PRINCIPAL DISPLAY PANEL - 5 Vial Package - yf vax 03

PRINCIPAL DISPLAY PANEL - 5 Vial Package - yf vax 03

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.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.