OTC - ACTIVE INGREDIENT SECTION
MEDICAGO SATIVA WHOLE
CHICORY ROOT
GLUCOSAMINE HYDROCHLORIDE
BUCKWHEAT
TEA LEAF
MORUS ALBA LEAF
LICORICE
FU LING
COIX LACRYMA-JOBI SEED
ANSERINE
Gout Relief 3310A Plus
- Manufacturer
- Bispit Canada Ltd.
- Effective date
- 2025-09-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:34:57
Label at a glance#
ProductGout Relief 3310A Plus
Active ingredientLICORICE, MEDICAGO SATIVA WHOLE, BUCKWHEAT, FU LING, CHICORY ROOT, MORUS ALBA LEAF, ANSERINE, TEA LEAF, COIX LACRYMA-JOBI SEED, GLUCOSAMINE HYDROCHLORIDE
Label structure8 sections
Label contents#
Full prescribing information#
INACTIVE INGREDIENT SECTION
CALCIUM CARBONATE
SODIUM CHLORIDE
WARNINGS SECTION
Ulsing three bottles is generally effective fordissolving crystals (as crystal dissoiution takestime);
You should experience noticeable effects afterat least 21 days of conbnlous use,It is noral to experence increose in uric acidlevels or gout recurrencelchanges imn affectedareas during the early days of use;Refrain from olcohol consumption, or limit itsionificantly, for at least 15 days before takingthis product;
lt has an auxiliary effect on improving libidoand supporting prostate health,
Do not use if you have a seafood allergy.
Store properly and out of reach of children.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Store properly and out of reach of children.
OTC - PURPOSE SECTION
This product is a pure plant extract; it canreduce the frequency of goutattacks; dissolve the crystals in thejoints; promote the excretion of blood uricacids,andimprove the purine metabolismand excretory system.
DOSAGE & ADMINISTRATION SECTION
2 tablets in the momingand 2 toblets in the evening.
INDICATIONS & USAGE SECTION
Applicable Population:patient with gout,high uric acid, depositionof urate crystal, kidney stone and bladder
stone.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85631-009-01 | Gout Relief 3310A Plus | 1 g in 1 CAPSULE | TABLET | 1 | 2 | |
| 85631-009-01 | Gout Relief 3310A Plus | 60 in 1 BOX | TABLET | 60 | 2 |
Products#
Every source-derived product name is available through these pages.
- Gout Relief 3310A Plus
- LICORICE
- MEDICAGO SATIVA WHOLE
- BUCKWHEAT
- FU LING
- CHICORY ROOT
- MORUS ALBA LEAF
- ANSERINE
- TEA LEAF
- CALCIUM CARBONATE
- COIX LACRYMA-JOBI SEED
- GLUCOSAMINE HYDROCHLORIDE
- GLUCOSAMINE
- SODIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 85631-009 | 85631-009-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LICORICE | 61ZBX54883 | ACTIB |
| MEDICAGO SATIVA WHOLE | DJO934BRBD | ACTIB |
| BUCKWHEAT | N0Y68724R3 | ACTIB |
| FU LING | XH37TWY5O4 | ACTIB |
| CHICORY ROOT | 090CTY533N | ACTIB |
| MORUS ALBA LEAF | M8YIA49Q2P | ACTIB |
| ANSERINE | HDQ4N37UGV | ACTIB |
| TEA LEAF | GH42T47V24 | ACTIB |
| CALCIUM CARBONATE | H0G9379FGK | IACT |
| COIX LACRYMA-JOBI SEED | 4Q4V6NTZ1F | ACTIB |
| GLUCOSAMINE HYDROCHLORIDE | 750W5330FY | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Gout Relief 3310A Plus | GOUT RELIEF 3310A PLUS | Bispit Canada Ltd. | 3e0a4e26-61b6-01cb-e063-6294a90a4efc | 2025-09-06 | Warnings | 85631-009-01 85631-009 85631000901 3e1d060f-1584-3b66-e063-6394a90a5996 3e0a4e26-61b6-01cb-e063-6294a90a4efc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.