Nithiodote Kit
Product Images NDC 60267-812

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 Nithiodote (NDC 60267-812). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hope 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

Chemical Structure (Nithiodote 01)

Chemical Structure (Nithiodote 01)
Chemical structure diagram of sodium nitrite, showing its atomic composition and bonding.*
FDA Label Image

Chemical Structure (Nithiodote 02)

Chemical Structure (Nithiodote 02)
Chemical structure of sodium thiosulfate pentahydrate, showing the central sulfur atoms bonded to oxygen atoms and two sodium ions, along with five water molecules of hydration.*
FDA Label Image

Principal Display Panel (Kit Carton)

Principal Display Panel (Kit Carton)
NITHIODOTE kit packaging label for Sodium Nitrite Injection, USP and Sodium Thiosulfate Injection, USP. The label indicates intravenous use, single use only. The kit contains 300 mg/10 mL Sodium Nitrite Injection and 12.5 grams/50 mL Sodium Thiosulfate Injection. Manufactured by Hope Pharmaceuticals. The label includes dosage and administration instructions for adults and children, storage information, and safety warnings.*

* 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.