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

Product Visual Gallery

This gallery contains 9 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

Serialized Pouch (51662 1537 2 Serialized Pouch Labeling Resized)

Label for VITAMIN K1 PHYTONADIONE injectable emulsion. The label states strength as 1 mg per 0.5 mL ampule for neonatal use. It includes NDC 51662-1537-2, lot number 123456, and expiration date 2025-01-01. The product is manufactured by HF Acquisition Co., LLC in Mukilteo, WA. The label instructs protection from light and storage at controlled room temperature.*

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

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

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

Logo (Hs Logo)

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

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

Box Labeling (Vitamin K 51662153734 Hf Serialized Case Label Image)

Label for Vitamin K1 Phytonadione Injectable Emulsion, with a strength of 1 mg per 0.5 mL neonatal concentration ampules. The label includes the NDC 51662-1537-3, lot number 123456, and expiration date 2025-01-01. It warns to protect from light and notes administration routes as intramuscular, subcutaneous, or intravenous. The label lists excipients including polyoxyethylated fatty acid derivative, dextrose, and benzyl alcohol and specifies storage at 20 to 25°C. Manufactured by HF Acquisition Co., LLC in Mukilteo, WA.*

FDA Label Image

Rfid Serialized Labeling (Vitamin K 51662153734 Hf Serialized Rfid Label Image)

A close-up image of a white label featuring a DataMatrix barcode and human-readable text. The label includes identifiers such as (01)00351662153734, (17)250101, and (10)123456. The text also instructs to see the manufacturer's package insert and notes distribution by HF Acquisition Co., LLC, Mukilteo, WA 98275. This label is associated with Vitamin K1 Phytonadione injection emulsion.*

* 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.