FDA.reportPublic FDA data

URICOZEN

Manufacturer
HCBIOPHARM
Effective date
2026-03-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:38:11

Label at a glance#

ProductURICOZEN
Active ingredientLONICERA JAPONICA FLOWER, PORTULACA OLERACEA WHOLE, WOLFIPORIA COCOS WHOLE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Portulaca oleracea 1X

Lonicera japonica 1X

Wolfiporia cocos 1X

OTC - PURPOSE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Take two (2) capsules twice a day. If severe, take two (2) capsules three times a day.

INDICATIONS & USAGE SECTION

To recover from gout*

To dissolve gout crystals*

To relieve joint pain and joint inflammation*

INACTIVE INGREDIENT SECTION

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 SECTION

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

uricozenuricozen

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80353-900-01URICOZEN1 in 1 BOTTLE, GLASSCAPSULE13
80353-900-02URICOZEN60 in 1 CAPSULECAPSULE603

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80353-90080353-900-02, 80353-900-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
GARDENIA JASMINOIDES FRUIT7CTH8MD549IACT
LONICERA JAPONICA FLOWER4465L2WS4YACTIB
POLYGONATUM ODORATUM ROOTKPF03O64AZIACT
PAULLINIA CUPANA WHOLEZN61XGA9AZIACT
CINNAMON5S29HWU6QBIACT
LYCIUM CHINENSE FRUITTG711Q7A1QIACT
MYRISTICA FRAGRANS WHOLEMF7T8BM40AIACT
ROSA DAVURICA WHOLE2HX1340941IACT
PORTULACA OLERACEA WHOLED5J3623SV2ACTIB
WOLFIPORIA COCOS WHOLEY1I7Z6FF4RACTIB
RUBUS COREANUS FRUIT18VM55XVF7IACT
DIOSCOREA JAPONICA ROOTI43FCF3356IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
URICOZENGOUT RECOVERY, JOINT PAIN AND INFLAMMATION RELIEF, AND GOUT CRYSTAL DISSOLUTIONHCBIOPHARM0bfb4b71-8392-15fa-e063-6394a90a771b2026-03-30WarningsExact identifier
ndc (package): 80353-900-02
ndc (package): 80353-900-01
ndc (product): 80353-900
ndc11 (package): 80353090001
ndc11 (package): 80353090002
spl id: 4e3936d2-03a5-6a63-e063-6394a90ad1b9
spl set id: 0bfb4b71-8392-15fa-e063-6394a90a771b

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.