Label: URICOZEN- gout recovery, joint pain and inflammation relief, and gout crystal dissolution capsule

  • NDC Code(s): 80353-900-01, 80353-900-02
  • Packager: HCBIOPHARM
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated December 8, 2023

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    Portulaca oleracea 1X

    Lonicera japonica 1X

    Wolfiporia cocos 1X

  • PURPOSE

    Recovers from gout symptoms such as gout crystals, joint pain, and inflammation*

  • 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.

  • PRINCIPAL DISPLAY PANEL

    Uricozen

  • INGREDIENTS AND APPEARANCE
    URICOZEN 
    gout recovery, joint pain and inflammation relief, and gout crystal dissolution capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80353-900
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) (LONICERA JAPONICA FLOWER - UNII:4465L2WS4Y) LONICERA JAPONICA FLOWER1 [hp_X]
    PORTULACA OLERACEA WHOLE (UNII: D5J3623SV2) (PORTULACA OLERACEA WHOLE - UNII:D5J3623SV2) PORTULACA OLERACEA WHOLE1 [hp_X]
    WOLFIPORIA COCOS WHOLE (UNII: Y1I7Z6FF4R) (WOLFIPORIA COCOS WHOLE - UNII:Y1I7Z6FF4R) WOLFIPORIA COCOS WHOLE1 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    GARDENIA JASMINOIDES FRUIT (UNII: 7CTH8MD549)  
    POLYGONATUM ODORATUM ROOT (UNII: KPF03O64AZ)  
    CINNAMON (UNII: 5S29HWU6QB)  
    LYCIUM CHINENSE FRUIT (UNII: TG711Q7A1Q)  
    MYRISTICA FRAGRANS WHOLE (UNII: MF7T8BM40A)  
    ROSA DAVURICA WHOLE (UNII: 2HX1340941)  
    RUBUS COREANUS FRUIT (UNII: 18VM55XVF7)  
    DIOSCOREA JAPONICA ROOT (UNII: I43FCF3356)  
    PAULLINIA CUPANA WHOLE (UNII: ZN61XGA9AZ)  
    Product Characteristics
    ColorgreenScoreno score
    ShapeCAPSULESize22mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80353-900-011 in 1 BOTTLE, GLASS12/07/2023
    1NDC:80353-900-0260 in 1 CAPSULE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/07/2023
    Labeler - HCBIOPHARM (042860151)