Arsenic Trioxide Injection, Solution
Product Images NDC 55150-366

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Arsenic Trioxide (NDC 55150-366). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us 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.

FDA Label Image

Chemical Structure (Arsenic Trioxide Str)

Chemical structure diagram showing a cyclic arsenic-oxygen compound corresponding to arsenic trioxide. The structure features arsenic atoms connected by oxygen atoms forming a ring-like arrangement.*

FDA Label Image

Arsenic-trioxide-fig1 (Arsenic Trioxide Fig1)

The label for Arsenic Trioxide Injection, 12 mg per 6 mL (2 mg/mL) single-dose vial for intravenous use. It includes warnings that it is a cytotoxic agent and instructs to discard unused portions. Distributed by AuroMedics Pharma LLC, made in Taiwan. The NDC is 55150-366-01.*

FDA Label Image

Package Label-principal Display Panel-12 mg Per 6 mL (2 mg/ml) (Container Label)

ARSENIC TRIOXIDE Injection 12 mg per 6 mL (2 mg/mL) carton, labeled for intravenous use only. The package contains 10 x 6 mL single-dose vials and is distributed by AuroMedics Pharma LLC. The label includes storage instructions and notes the product is a cytotoxic agent with no preservatives. NDC 55150-366-10 is visible.*

FDA Label Image

Package Label-principal Display Panel-12 mg Per 6 mL (2 mg/ml) (Container-Carton (10 Vials))

Packaging label for Arsenic Trioxide Injection 12 mg per 6 mL (2 mg/mL) intravenous injection by Eugia US LLC. The carton contains 10 single-dose 6 mL vials. It includes storage instructions, cytotoxic agent warning, distributor information, and states the vial stopper is not made with natural rubber latex. The product NDC is 55150-366-10.*

* 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.