Chemical Structure (Nithiodote 01)
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.
Product Images & Figures Index
Chemical Structure (Nithiodote 02)
Principal Display Panel (Kit Carton)
NITHIODOTE is a medication containing Sodium Nitrite Injection, USP and Sodium Thiosulfate Injection, USP for intravenous use. It is a single-use only medication, and any unused portion should be discarded. The medication is used for emergency purposes, and medical personnel using the kit should be trained in advance. The medication should be visually inspected for particle matters and discoloration before use, and the temperature should be maintained between 20°C and 25°C. The dosage varies based on the intravenous dose of Sodium Nitrite and Sodium Thiosulfate, and the medication comes in a box that contains Sodium Nitrite Injection, USP 300 mg/10 mL and Sodlum Thiosulfate Injection, USP 12.5 grams/50 mL.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
