GOUT RELIEF 3310-S- celery seed, medicago sativa whole,chicory root capsule

Gout Relief 3310-S by

Drug Labeling and Warnings

Gout Relief 3310-S by is a Homeopathic medication manufactured, distributed, or labeled by Bispit Canada Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

CELERY SEED 1G1EAA320L 20.00%
MEDICAGO SATIVA WHOLE DJO934BRBD 20.00%
CHICORY ROOT 090CTY533N 18.00%
GLUCOSAMINE HYDROCHLORIDE 750W5330FY 10.00%
BUCKWHEAT N0Y68724R3 7.00%
TEA LEAF GH42T47V24 5.00%
PUERARIN Z9W8997416 5.00%
MORUS ALBA LEAF M8YIA49Q2P 3.00%
LICORICE 61ZBX54883 0.20%
SODIUM CHLORIDE 451W47IQ8X 2.00%

PURPOSE

This product has a significanteffect on gout, crystal deposits,and hyperuricemia;
elt has an auxiliary effectof mitigating kidney stonesand bladder stones

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

DOSAGE & ADMINISTRATION

The product has great somatosensation after taking it atleast 21 days in the earty stage;3. Elevated uric acid or gout recurrence and site changes arenoral in the earty stage of taking this product;

INDICATIONS & USAGE

Dissolved CrystallizationKidney StoneGallstone< Urinary Calculus

WARNINGS

For your health, please read the followingcarefully
1. The use of three vials can effectivety dissolve crystallization (ittakes time to dissolve crystallization);2. The product has great somatosensation after taking it atleast 21 days in the early stage;3. Elevated uric acid or gout recurrence and site changes arenormal in the early stage of taking this product;4. Try not to drink alcohol or drink less 15 days before takingthis product;
5. This product certainly has significant effect on gout,crystallization and hyperuricemia;

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.

INACTIVE INGREDIENT

MICROCRYSTALLINE CELLULOSE
MALTOSYL-ISOMALTOTETRAOSE
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED
MAGNESIUM STEARATE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GOUT RELIEF 3310-S 
celery seed, medicago sativa whole,chicory root capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85631-003
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) (GLUCOSAMINE - UNII:N08U5BOQ1K)	GLUCOSAMINE HYDROCHLORIDE	130 mg  in 1.3 g
MORUS ALBA LEAF (UNII: M8YIA49Q2P) (MORUS ALBA LEAF - UNII:M8YIA49Q2P)	MORUS ALBA LEAF	39 mg  in 1.3 g
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	26 mg  in 1.3 g
MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (MEDICAGO SATIVA WHOLE - UNII:DJO934BRBD)	MEDICAGO SATIVA WHOLE	260 mg  in 1.3 g
TEA LEAF (UNII: GH42T47V24) (TEA LEAF - UNII:GH42T47V24)	TEA LEAF	65 mg  in 1.3 g
CELERY SEED (UNII: 1G1EAA320L) (CELERY SEED - UNII:1G1EAA320L)	CELERY SEED	260 mg  in 1.3 g
CHICORY ROOT (UNII: 090CTY533N) (CHICORY ROOT - UNII:090CTY533N)	CHICORY ROOT	234 mg  in 1.3 g
PUERARIN (UNII: Z9W8997416) (PUERARIN - UNII:Z9W8997416)	PUERARIN	65 mg  in 1.3 g
BUCKWHEAT (UNII: N0Y68724R3) (BUCKWHEAT - UNII:N0Y68724R3)	BUCKWHEAT	91 mg  in 1.3 g
LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883)	LICORICE	2.6 mg  in 1.3 g

Inactive Ingredients
Ingredient Name	Strength
CELLULOSE GUM (UNII: K679OBS311)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
MALTOSYL-ISOMALTOTETRAOSE (UNII: B9HR7A9UFR)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	score with uneven pieces
Shape	CAPSULE	Size	20mm
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85631-003-01	60 in 1 BOX	07/28/2025
1		1.3 g in 1 CAPSULE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/28/2025

Labeler - Bispit Canada Ltd. (243332192)

Registrant - Bispit Canada Ltd. (243332192)