Vitamin K1 - Phytonadione Injection, Emulsion
Product Images NDC 51662-1536

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Vitamin K1 - Phytonadione (NDC 51662-1536). 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

Pouch Labeling (51662 1536 2 Pouch Labeling)

Label of VITAMIN K1 - PHYTONADIONE injectable emulsion 10 mg/mL in a 1 mL ampule. The label shows the product name, strength, dosage form, NDC 51662-1536-2, lot number 123456, expiration date 01/2030, and manufacturer information for HF Acquisition Co LLC, Mukilteo, WA.*

FDA Label Image

Box Labeling (51662 1536 3 Box Labeling)

Label for VITAMIN K1 - PHYTONADIONE injectable emulsion, USP 10 mg/mL in 1 mL ampules, sold in a box of 25. The label includes the NDC 51662-1536-3, lot number 123456, and expiration date 2030-01-01. Manufactured by HF Acquisition Co., LLC in Mukilteo, WA. Storage and handling instructions are partially visible.*

FDA Label Image

Serialized Labeling (51662 1536 3 Serialized Labeling)

The image shows a small white label with a QR code and several identifiers including a GTIN, lot number, and expiration date. It indicates the product is distributed by HF Acquisition Co., LLC in Mukilteo, WA. The label is for VITAMIN K1 - PHYTONADIONE injection emulsion, 10 mg/mL, prescription only, distributed by HF Acquisition Co LLC DBA HealthFirst.*

FDA Label Image

Boxed Warning (Boxed Warning)

This text panel contains a warning regarding severe reactions, including fatalities, associated with intravenous and intramuscular use of phytonadione injection. It advises caution and restricts these administration routes to situations where subcutaneous use is not feasible and serious risk is justified.*

FDA Label Image

Dosage (D And A)

A dosage guideline table for Vitamin K1 Injection (Phytonadione Injectable Emulsion, USP) showing dosage recommendations. It includes neonatal dosages for hemorrhagic disease prophylaxis and treatment, and adult initial dosages for anticoagulant-induced prothrombin deficiency and hypoprothrombinemia caused by other factors. Dosage amounts range from 0.5 mg to 50 mg with various routes of administration noted.*

FDA Label Image

How Supplied (How Supplied)

A data table presenting Vitamin K1 Injection (Phytonadione Injectable Emulsion, USP) units of sale and concentrations. It shows two NDCs: 0409-9157-01 for a bundle of 5 clamcells each containing 5 single-dose ampuls at 1 mg/0.5 mL concentration, and 0409-9158-01 for a similar bundle at 10 mg/mL concentration. Additional storage instructions and distributor information from Hospira, Inc. are included below the table.*

FDA Label Image

Inner Amp (Inner Ampule Labeling)

Label for Vitamin K1 Injection, Phytonadione Injectable Emulsion, USP, 10 mg/mL single-dose ampul. The label indicates administration routes as intramuscular, subcutaneous, or intravenous. It includes storage instructions, contents, and the distributor Hospira, Inc., Lake Forest, IL. The label displays NDC numbers and a barcode.*

FDA Label Image

Outer Amp (Outer Ampule Labeling)

Label for VITAMIN K1 injection (Phytonadione Injectable Emulsion, USP) 10 mg/mL. The label indicates 1 mL vial size and includes a note on aluminum content and light protection. Distributed by Hospira, Inc. in Lake Forest, IL, USA. The label features an NDC barcode with code 0409-9158-31.*

FDA Label Image

Structure (Structure)

Chemical structure diagram depicting the molecular structure of Vitamin K1 (Phytomenadione, Phytonadione) as shown in the image, illustrating its organic compound framework with rings and side chains.*

* 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.