Home NDC 85631-001 Gout Relief 3310-S
Product NDC 85631-001
11-digit product format 856310001
Labeler code 85631
Product ID 85631-001_346f68ea-73ab-99c6-e063-6394a90af5d5
Type HUMAN OTC DRUG
Nonproprietary name CELERY SEED MEDICAGO SATIVA WHOLE
Dosage form CAPSULE
Route ORAL
Labeler Bispit Canada Ltd.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-05-06
Substance BUCKWHEAT; CELERY SEED; CHICORY ROOT; GLUCOSAMINE HYDROCHLORIDE; LICORICE; LYSIMACHIA CHRISTINAE WHOLE; MEDICAGO SATIVA WHOLE; MORUS ALBA LEAF; PUERARIN; SODIUM CHLORIDE
Active strength 90; 260; 230; 130; 2.6; 65; 260; 39; 65; 26 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], Cell-mediated Immunity [PE], Dietary Proteins [CS], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC]
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 LYSIMACHIA CHRISTINAE WHOLE 90 mg/1.3g MEDICAGO SATIVA WHOLE 260 mg/1.3g PUERARIN 230 mg/1.3g SODIUM CHLORIDE 130 mg/1.3g CHICORY ROOT 2.6 mg/1.3g GLUCOSAMINE HYDROCHLORIDE 65 mg/1.3g BUCKWHEAT 260 mg/1.3g LICORICE 39 mg/1.3g CELERY SEED 65 mg/1.3g MORUS ALBA LEAF 26 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 85631-001-01 Gout Relief 3310-S 1.3 g in 1 CAPSULE CAPSULE 1.3 1 85631-001-01 Gout Relief 3310-S 60 in 1 BOTTLE CAPSULE 60 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 85631-001 GOUT RELIEF 3310-S (CELERY SEED MEDICAGO SATIVA WHOLE) CAPSULE [BISPIT CANADA LTD.] 1 Current NDC, 2 package rows 20250507_346f68ea-73aa-99c6-e063-6394a90af5d5.zip
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 85631-001-01 85631000101 60 CAPSULE in 1 BOTTLE (85631-001-01) / 1.3 g in 1 CAPSULE 60 capsule 2025-05-06 No No Current