Oxytocin Injection, Solution
Product Images NDC 65219-021

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxytocin (NDC 65219-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Structure (Oxy0c 0000 01)

Structure (Oxy0c 0000 01)
Chemical structure diagram showing the peptide sequence of oxytocin, listing the amino acids and their order with some side-chain details represented by chemical groups and bonds.*
FDA Label Image

Logo (Oxy0c 0000 02)

Logo (Oxy0c 0000 02)
FDA Label Image

Package Label – Principal Display – Oxytocin Injection, Usp 10 Usp Unit Per mL Vial Label (Oxy0c 0000 03)

Package Label – Principal Display – Oxytocin Injection, Usp 10 Usp Unit Per mL Vial Label (Oxy0c 0000 03)
Label for Oxytocin Injection, USP (Synthetic) 10 USP Units per mL in 1 mL single dose vial. The label indicates use for intravenous infusion or intramuscular use. It is marked Rx only and instructs to discard unused portions. Labeler is Fresenius Kabi USA, LLC. Includes NDC 65219-021-00 and barcode.*
FDA Label Image

Package Label – Principal Display – Glycopyrrolate Injection, Usp 0.2 mg Per mL Tray Label (Oxy0c 0000 04)

Package Label – Principal Display – Glycopyrrolate Injection, Usp 0.2 mg Per mL Tray Label (Oxy0c 0000 04)
Oxytocin Injection, USP (Synthetic) label for 10 USP Units per mL in 1 mL single dose vials. The label is marked for intravenous infusion or intramuscular use and indicates 25 single dose vials per package. It includes storage instructions, sterility notice, and the manufacturer Fresenius Kabi USA, LLC, Lake Zurich, IL, with product NDC 65219-021.*

* 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.