Phytonadione Injection, Emulsion
Product Images NDC 81607-020

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Phytonadione (NDC 81607-020). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Orbicular Pharmaceutical Technologies Private Limited, 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

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FDA Label Image

Image (1a12da69 249c 42d2 8cde 1f0ecfbc299c 02)

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This text provides instructions on how to administer an injection using a safety shield device. It includes steps such as removing the needle cover, expelling air, activating the safety shield, and administering the injection following aseptic technique. It emphasizes the importance of proper positioning of the safety shield and one-handed technique for activating it. Additionally, it mentions the need for a gentle and quick motion to activate the safety shield until an audible click is heard.*
FDA Label Image

Container Label (1a12da69 249c 42d2 8cde 1f0ecfbc299c 03)

Container Label (1a12da69 249c 42d2 8cde 1f0ecfbc299c 03)
This is a description for a pharmaceutical product. It appears to be a single-dose injection of Phytonadione, an emulsion made in India. The product is intended for neonatal use and can be administered intravenously, intramuscularly, or subcutaneously with caution. The text also provides specific lot and expiration details for tracking and safety purposes.*
FDA Label Image

Mono Carton Label (1a12da69 249c 42d2 8cde 1f0ecfbc299c 04)

Mono Carton Label (1a12da69 249c 42d2 8cde 1f0ecfbc299c 04)
This text provides information about Phytonadione Injectable Emulsion, USP, a medication containing Vitamin K used for intravenous, intramuscular, or subcutaneous administration. The text includes details about the composition of the medication, storage instructions, dosage information, and the manufacturer information. Additionally, it mentions the prefilled syringe with a 27 G. x 1/2" needle for administering the medication. The medication is indicated for neonatal concentration and is single-dose, with unused portions recommended to be discarded.*
FDA Label Image

Outer Carton Label (1a12da69 249c 42d2 8cde 1f0ecfbc299c 05)

Outer Carton Label (1a12da69 249c 42d2 8cde 1f0ecfbc299c 05)
This is information about a batch coding and barcode GTIN: X000000000000K for a 205 mL container with 1 mg of MFix. It contains ingredients like polysorbate 80, propylene, glacial acetic acid, and Phytonadione Injectable Emulsion. The product is in prefilled syringes with 27 G, X/2" needles for intravenous, intramuscular, or subcutaneous use. A user guide is included in the carton, and storage temperatures are specified for the medication. It is a single-dose product with no preservatives. The usual dosage should be checked on the insert.*
FDA Label Image

User Guide Image (1a12da69 249c 42d2 8cde 1f0ecfbc299c 06)

User Guide Image (1a12da69 249c 42d2 8cde 1f0ecfbc299c 06)
This is a user guide for a prefilled syringe with safety shield containing phytonadione injectable emulsion, USP. The guide emphasizes the importance of using an aseptic technique and provides detailed instructions on handling and administering the injection. It includes information on checking the expiration date, inspecting the medicine, and activating the safety shield after injection. The text also includes safety precautions and guidelines for proper disposal of used syringes. The product is manufactured by Gland Pharma Limited in India.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.