Home NDC 85631-003 Gout Relief 3310-S
Product NDC 85631-003
11-digit product format 856310003
Labeler code 85631
Product ID 85631-003_3b610399-6dbe-c84f-e063-6394a90afd5e
Type HUMAN OTC DRUG
Nonproprietary name CELERY SEED, MEDICAGO SATIVA WHOLE,CHICORY ROOT
Dosage form CAPSULE
Route ORAL
Labeler Bispit Canada Ltd.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-07-28
Substance BUCKWHEAT; CELERY SEED; CHICORY ROOT; GLUCOSAMINE HYDROCHLORIDE; LICORICE; MEDICAGO SATIVA WHOLE; MORUS ALBA LEAF; PUERARIN; SODIUM CHLORIDE; TEA LEAF
Active strength 91; 260; 234; 130; 2.6; 260; 39; 65; 26; 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; 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], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [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 GLUCOSAMINE HYDROCHLORIDE 91 mg/1.3g MORUS ALBA LEAF 260 mg/1.3g LICORICE 234 mg/1.3g PUERARIN 130 mg/1.3g BUCKWHEAT 2.6 mg/1.3g SODIUM CHLORIDE 260 mg/1.3g MEDICAGO SATIVA WHOLE 39 mg/1.3g TEA LEAF 65 mg/1.3g CELERY SEED 26 mg/1.3g CHICORY ROOT 65 mg/1.3g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85631-003-01 Gout Relief 3310-S 1.3 g in 1 CAPSULE CAPSULE 1.3 2 85631-003-01 Gout Relief 3310-S 60 in 1 BOX CAPSULE 60 2
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 85631-003-01 85631000301 60 CAPSULE in 1 BOX (85631-003-01) / 1.3 g in 1 CAPSULE 60 capsule 2025-07-28 No No Current