URICOZEN

Product NDC
80353-900
11-digit product format
803530900
Labeler code
80353
Product ID
80353-900_4e3936d2-03a5-6a63-e063-6394a90ad1b9
Type
HUMAN OTC DRUG
Nonproprietary name
Gout recovery, Joint pain and inflammation relief, and gout crystal dissolution
Dosage form
CAPSULE
Route
ORAL
Labeler
HCBIOPHARM
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2023-12-07
Substance
LONICERA JAPONICA FLOWER; PORTULACA OLERACEA WHOLE; WOLFIPORIA COCOS WHOLE
Active strength
1; 1; 1 [hp_X]/1; [hp_X]/1; [hp_X]/1
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
URICOZEN
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LONICERA JAPONICA FLOWER1 [hp_X]/1
PORTULACA OLERACEA WHOLE1 [hp_X]/1
WOLFIPORIA COCOS WHOLE1 [hp_X]/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4465L2WS4YInternal UNII lookup
D5J3623SV2Internal UNII lookup
Y1I7Z6FF4RInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0bfb4b71-8392-15fa-e063-6394a90a771bAvailable on FDA.report

DailyMed Package Descriptions#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80353-900URICOZEN (GOUT RECOVERY, JOINT PAIN AND INFLAMMATION RELIEF, AND GOUT CRYSTAL DISSOLUTION) CAPSULE [HCBIOPHARM]2Current NDC, 2 package rows20250104_0bfb4b71-8392-15fa-e063-6394a90a771b.zip

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 (product): 80353-900

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
80353-900-01803530900011 CAPSULE in 1 BOTTLE, GLASS (80353-900-01) / 60 CAPSULE in 1 CAPSULE (80353-900-02) 1 capsule2023-12-07NoNoCurrent
80353-900-028035309000260 in 1 CAPSULEHistorical