Gout Relief 3310-S

Product NDC: 85631-006
11-digit product format: 856310006
Labeler code: 85631
Product ID: 85631-006_3dbf3436-16ba-b793-e063-6394a90a1e71
Type: HUMAN OTC DRUG
Nonproprietary name: MEDICAGO SATIVA WHOLE CHICORY ROOT
Dosage form: CAPSULE
Route: ORAL
Labeler: Bispit Canada Ltd.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2025-09-01
Substance: BUCKWHEAT; CHICORY ROOT; COIX LACRYMA-JOBI SEED; FU LING; GLUCOSAMINE HYDROCHLORIDE; LICORICE; MEDICAGO SATIVA WHOLE; MORUS ALBA LEAF; TEA LEAF
Active strength: 91; 299; 104; 26; 130; 2.6; 260; 169; 65 mg/1.3g; mg/1.3g; mg/1.3g; mg/1.3g; mg/1.3g; mg/1.3g; mg/1.3g; mg/1.3g; mg/1.3g
Pharmacologic classes: Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Gout Relief 3310-S
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
COIX LACRYMA-JOBI SEED	91 mg/1.3g
MEDICAGO SATIVA WHOLE	299 mg/1.3g
BUCKWHEAT	104 mg/1.3g
TEA LEAF	26 mg/1.3g
MORUS ALBA LEAF	130 mg/1.3g
CHICORY ROOT	2.6 mg/1.3g
FU LING	260 mg/1.3g
GLUCOSAMINE HYDROCHLORIDE	169 mg/1.3g
LICORICE	65 mg/1.3g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Q4V6NTZ1F	Internal UNII lookup
DJO934BRBD	Internal UNII lookup
N0Y68724R3	Internal UNII lookup
GH42T47V24	Internal UNII lookup
M8YIA49Q2P	Internal UNII lookup
090CTY533N	Internal UNII lookup
XH37TWY5O4	Internal UNII lookup
750W5330FY	Internal UNII lookup
61ZBX54883	Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
Identifier	FDA.report destination
3dbf3436-16b9-b793-e063-6394a90a1e71	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
85631-006-01	Gout Relief 3310-S	60 in 1 BOTTLE	CAPSULE	60		1
85631-006-01	Gout Relief 3310-S	1.3 g in 1 CAPSULE	CAPSULE	1.3		1

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Gout Relief 3310-S	MEDICAGO SATIVA WHOLE CHICORY ROOT	Bispit Canada Ltd.	3dbf3436-16b9-b793-e063-6394a90a1e71	2025-09-01	Warnings	Exact identifier ndc (product): 85631-006

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
N0Y68724R3	BUCKWHEAT		BUCKWHEAT
090CTY533N	CHICORY ROOT		CHICORY ROOT
4Q4V6NTZ1F	COIX LACRYMA-JOBI SEED		COIX LACRYMA-JOBI SEED
XH37TWY5O4	FU LING		FU LING
750W5330FY	GLUCOSAMINE HYDROCHLORIDE	66-84-2	GLUCOSAMINE HYDROCHLORIDE
61ZBX54883	LICORICE		LICORICE
M8YIA49Q2P	MORUS ALBA LEAF		MORUS ALBA LEAF
GH42T47V24	TEA LEAF		TEA LEAF

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
85631-006-01	85631000601	60 CAPSULE in 1 BOTTLE (85631-006-01) / 1.3 g in 1 CAPSULE	60 capsule	2025-09-01	No	No	Current