Arsenic Trioxide Injection
Product Images NDC 25021-227

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Arsenic Trioxide (NDC 25021-227). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceuticals, 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

Structural Formula (Ars05 0001 01)

Structural Formula (Ars05 0001 01)
Chemical structure diagram of arsenic trioxide showing the arrangement of arsenic and oxygen atoms in the molecule.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Ars05 0001 02)

Package Label – Principal Display Panel – Vial Label (Ars05 0001 02)
Arsenic Trioxide Injection 10 mg per 10 mL (1 mg per mL) single-dose vial label. For intravenous use only. Manufactured for Sagent Pharmaceuticals, Schaumburg, IL. Includes caution indicating it is a cytotoxic agent. Storage and handling instructions note it is sterile, nonpyrogenic with a preservative-free content, and contains natural rubber latex. The label displays the NDC 25021-226-10 and barcode.*
FDA Label Image

Package Label – Principal Display Panel – Vial Label (Ars05 0001 03)

Package Label – Principal Display Panel – Vial Label (Ars05 0001 03)
Arsenic Trioxide Injection label showing 12 mg per 6 mL (2 mg per mL) strength in a 6 mL single-dose vial for intravenous use. The label notes it as a cytotoxic agent and sterile, nonpyrogenic with preservative-free packaging. Manufactured for Sagent Pharmaceuticals, Schaumburg, IL, and made in India.*

* 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.