"85631-009-01" National Drug Code (NDC)

NDC Code	85631-009-01
Package Description	60 CAPSULE in 1 BOX (85631-009-01) / 1 g in 1 CAPSULE
Product NDC	85631-009
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Gout Relief 3310a Plus
Non-Proprietary Name	Gout Relief 3310a Plus
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20250905
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Bispit Canada Ltd.
Substance Name	ANSERINE; BUCKWHEAT; CHICORY ROOT; COIX LACRYMA-JOBI SEED; FU LING; GLUCOSAMINE HYDROCHLORIDE; LICORICE; MEDICAGO SATIVA WHOLE; MORUS ALBA LEAF; TEA LEAF
Strength	350; 40; 180; 40; 10; 70; 1; 150; 75; 34
Strength Unit	mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g; mg/g
Pharmacy 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]