Phytonadione Injection, Emulsion
Product Images NDC 0404-9969

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Phytonadione (NDC 0404-9969). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

Formula1.jpg (Formula1)

Chemical structure of phytonadione, the active ingredient in PHYTONADIONE 10 mg/mL injection emulsion by Henry Schein, Inc. The diagram shows the molecular structure including aromatic rings and side chains typical of the vitamin K1 chemical composition.*

FDA Label Image

Image1.jpg (Image1)

A dosage guideline table for phytonadione injectable emulsion, USP. It details dosages for newborns and adults, including prophylaxis and treatment for newborns, and initial dosages for adults with anticoagulant-induced prothrombin deficiency and hypoprothrombinemia due to various causes.*

FDA Label Image

Image2.jpg (Image2)

Data tables showing product packaging and details for phytonadione injectable emulsion. The carton contains 25 ampules of 1 mL each with NDC 43598-405-16. Each 1 mL ampule contains 10 mg of phytonadione at a concentration of 10 mg/mL, with NDC 43598-405-11.*

FDA Label Image

Label1.jpg (Label1)

Label for PHYTONADIONE 10 mg/mL injectable emulsion, USP in a single dose ampule. The label indicates use for intramuscular, subcutaneous, or intravenous administration. Includes storage instructions to protect from light and keep ampule in bag until use. Manufacturer is Henry Schein, Inc., located in Bastian, VA. The label also contains lot number, expiration date placeholders, an NDC barcode, and a QR code.*

* 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.