Otc - Active Ingredient
chicory extract powder, aronia extract powder, kelp extract powder
Cyanox
FDA Label NDC 72173-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jbklab Co., Ltd for the product Cyanox (NDC 72173-0001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, warnings, otc - keep out of reach of children, indications & usage, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Natural raspberry flavor, enzyme treated stevia
Otc - Purpose
• Application for a patent : Adjuvants and anticancer immuno-therapeutic agents comprising anthoyanin- fucoidan complex
• Registration of a patent : Anthocyanin via Charge Complex with Anionic Polysaccharide Having Improved Stability, Composition Containing the Same, and Method for Preparing the Same
Warnings
• Application for a patent : Adjuvants and anticancer immuno-therapeutic agents comprising anthoyanin- fucoidan complex
• Registration of a patent : Anthocyanin via Charge Complex with Anionic Polysaccharide Having Improved Stability, Composition Containing the Same, and Method for Preparing the Same
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Indications & Usage
Take 1 stick once a time, and twice a day
Dosage & Administration
for oral use only
Package Label.Principal Display Panel
Label (Label)
* Please review the disclaimer below.
