Otc - Active Ingredient
Portulaca oleracea 1X
Lonicera japonica 1X
Wolfiporia cocos 1X
Uricozen Capsule
FDA Label NDC 80353-900
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hcbiopharm for the product Uricozen (NDC 80353-900). 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, otc - purpose, otc - keep out of reach of children, dosage & administration, indications & usage, inactive ingredient, warnings, other safety information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Recovers from gout symptoms such as gout crystals, joint pain, and inflammation*
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Dosage & Administration
Take two (2) capsules twice a day. If severe, take two (2) capsules three times a day.
Indications & Usage
To recover from gout*
To dissolve gout crystals*
To relieve joint pain and joint inflammation*
Inactive Ingredient
Cape Jasmine (Gardenia jasminoides) Fruit, Solomon's Seal (Polygonatum odoratum) Root, Cinnamon, Goji Berry (Lycium chinense) Fruit, Nutmeg (Myristica fragrans), Amur Rose (Rosa davurica), Korean Black Raspberry (Rubus coreanus) Fruit, Mountain Yam (Dioscorea japonica) Root, Guarana (Paullinia cupana)
Warnings
Individuals with known medical conditions should consult a doctor prior to using this.
Other Safety Information
Do not use if seal is broken.
Do not eat freshness packet enclosed.
Keep out of direct sunlight, high temperature, and humidity.
Store in a cool, dry place.
Package Label.Principal Display Panel
Uricozen (Uricozen)
* Please review the disclaimer below.
