GOUT RELIEF 3310-S- celery seed medicago sativa whole 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
MEDICAGO SATIVA WHOLE
CHICORY ROOT
GLUCOSAMINE HYDROCHLORIDE
BUCKWHEAT
LYSIMACHIA CHRISTINAE WHOLE
PUERARIN
MORUS ALBA LEAF
LICORICE
SODIUM CHLORIDE

PURPOSE

Farewell To Gout

lmprove Metabolism

Balance Uric Acid

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

DOSAGE & ADMINISTRATION

2. 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

Long-term administration of the product:1、Auxiliary effect on improving sexual desire and strengtheningprostate problems;
2、Auxiliary effect on kidney stones and bladder stones;

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

85631-001-01

INGREDIENTS AND APPEARANCE

GOUT RELIEF 3310-S 
celery seed medicago sativa whole capsule

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85631-001
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LYSIMACHIA CHRISTINAE WHOLE (UNII: 2HI4019I96) (LYSIMACHIA CHRISTINAE WHOLE - UNII:2HI4019I96)	LYSIMACHIA CHRISTINAE WHOLE	65 mg  in 1.3 g
MEDICAGO SATIVA WHOLE (UNII: DJO934BRBD) (MEDICAGO SATIVA WHOLE - UNII:DJO934BRBD)	MEDICAGO SATIVA WHOLE	260 mg  in 1.3 g
PUERARIN (UNII: Z9W8997416) (PUERARIN - UNII:Z9W8997416)	PUERARIN	65 mg  in 1.3 g
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	26 mg  in 1.3 g
CHICORY ROOT (UNII: 090CTY533N) (CHICORY ROOT - UNII:090CTY533N)	CHICORY ROOT	230 mg  in 1.3 g
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY) (GLUCOSAMINE - UNII:N08U5BOQ1K)	GLUCOSAMINE HYDROCHLORIDE	130 mg  in 1.3 g
BUCKWHEAT (UNII: N0Y68724R3) (BUCKWHEAT - UNII:N0Y68724R3)	BUCKWHEAT	90 mg  in 1.3 g
LICORICE (UNII: 61ZBX54883) (LICORICE - UNII:61ZBX54883)	LICORICE	2.6 mg  in 1.3 g
CELERY SEED (UNII: 1G1EAA320L) (CELERY SEED - UNII:1G1EAA320L)	CELERY SEED	260 mg  in 1.3 g
MORUS ALBA LEAF (UNII: M8YIA49Q2P) (MORUS ALBA LEAF - UNII:M8YIA49Q2P)	MORUS ALBA LEAF	39 mg  in 1.3 g

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

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: 85631-001-01	60 in 1 BOTTLE	05/06/2025
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		05/06/2025

Labeler - Bispit Canada Ltd. (243332192)

Registrant - Bispit Canada Ltd. (243332192)

Establishment
Name	Address	ID/FEI	Business Operations
Bispit Canada Ltd.		243332192	manufacture(85631-001)