Home NDC 85631-009 Gout Relief 3310A Plus
Product NDC 85631-009
11-digit product format 856310009
Labeler code 85631
Product ID 85631-009_3e1d060f-1584-3b66-e063-6394a90a5996
Type HUMAN OTC DRUG
Nonproprietary name Gout Relief 3310A Plus
Dosage form TABLET
Route ORAL
Labeler Bispit Canada Ltd.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2025-09-05
Substance ANSERINE; BUCKWHEAT; CHICORY ROOT; COIX LACRYMA-JOBI SEED; FU LING; GLUCOSAMINE HYDROCHLORIDE; LICORICE; MEDICAGO SATIVA WHOLE; MORUS ALBA LEAF; TEA LEAF
Active strength 350; 40; 180; 40; 10; 70; 1; 150; 75; 34 mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g
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 3310A Plus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LICORICE 350 mg/g MEDICAGO SATIVA WHOLE 40 mg/g BUCKWHEAT 180 mg/g FU LING 40 mg/g CHICORY ROOT 10 mg/g MORUS ALBA LEAF 70 mg/g ANSERINE 1 mg/g TEA LEAF 150 mg/g COIX LACRYMA-JOBI SEED 75 mg/g GLUCOSAMINE HYDROCHLORIDE 34 mg/g
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 Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 85631-009-01 Gout Relief 3310A Plus 1 g in 1 CAPSULE TABLET 1 2 85631-009-01 Gout Relief 3310A Plus 60 in 1 BOX TABLET 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 85631-009-01 85631000901 60 CAPSULE in 1 BOX (85631-009-01) / 1 g in 1 CAPSULE 60 capsule 2025-09-05 No No Current