Vitamin K1 Phytonadione Injection, Emulsion
Product Images NDC 51662-1537

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Vitamin K1 Phytonadione (NDC 51662-1537). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Boxed Warning (Boxed)

A warning text panel for Vitamin K1 Phytonadione injection, emulsion 2 mg/mL. It details severe reactions, including fatalities, occurring during or immediately after intravenous and intramuscular use, emphasizing caution with these routes and recommending restriction to situations where subcutaneous administration is not feasible due to serious risk.*

FDA Label Image

Structure (Structure)

Chemical structure of vitamin K1 (phytonadione) showing the fused benzene and cyclohexadienone ring with a long isoprenoid side chain containing multiple methyl groups and a terminal methyl group.*

FDA Label Image

Dosage (Dosage And Administration)

A table summarizing dosage guidelines for Vitamin K1 Injection (Phytonadione Injectable Emulsion, USP). It lists dosages for newborns and adults under various conditions, including hemorrhagic disease of the newborn, treatment considerations, and anticoagulant-induced prothrombin deficiency, with specific dosage amounts for intramuscular and subcutaneous administration.*

FDA Label Image

Hs (Hs)

A data table presenting unit of sale options and their concentrations for Vitamin K1, Phytonadione injections. It lists two NDC codes: 0409-9157-01, a bundle of five 1 mg/0.5 mL single-dose ampuls, and 0409-9158-01, a bundle of five 10 mg/mL single-dose ampuls.*

FDA Label Image

Logo (Hs Logo)

FDA Label Image

Label (51662 1537 2 Pouch Label3)

Label for Vitamin K1 Phytonadione Injectable Emulsion, USP, 1 mg per 0.5 mL ampul, labeled for neonatal concentration. The label includes product NDC 51662-1537-2, lot number 789210, and expiration date 2030-09-19. It indicates preservation, storage instructions, and manufacturer HF Acquisition Co LLC, Mukilteo, WA.*

FDA Label Image

Ampule (Ampule Label)

Label for Vitamin K1 (Phytonadione) injection emulsion, USP, neonatal concentration 1 mg/0.5 mL. The vial volume is 0.5 mL and the label includes cautionary storage instructions, distributor information (Hospira, Inc., Lake Forest, IL), and a barcode. The label is marked Rx only.*

FDA Label Image

Label (51662 1537 3 Case Label)

Label for Vitamin K1 Phytonadione Injectable Emulsion, USP 1 mg/0.5 mL neonatal concentration ampules, 25 per box. Includes NDC 51662-1537-3 and lot number 789210, with an expiration date of September 19, 2030. Manufactured by HF Acquisition Co., LLC, Mukilteo, WA. The product is a prescription injectable emulsion with directions for proper storage and usage.*

* 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.