"43689-0007-2" National Drug Code (NDC)

NDC Code	43689-0007-2
Package Description	1 BOTTLE in 1 CARTON (43689-0007-2) > 125 TABLET in 1 BOTTLE (43689-0007-1)
Product NDC	43689-0007
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Sciatica Relief
Non-Proprietary Name	Capsicum Annuum, Colocynthis, Gnaphalium Polycephalum, Magnesia Phosphorica,
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20121011
End Marketing Date	20230330
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Magni Company
Substance Name	CAPSICUM; CITRULLUS COLOCYNTHIS FRUIT PULP; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; PSEUDOGNAPHALIUM OBTUSIFOLIUM
Strength	6; 6; 6; 6
Strength Unit	[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacy Classes	Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vegetable Proteins [CS]