"71971-6030-5" National Drug Code (NDC)

NDC Code	71971-6030-5
Package Description	30 TABLET in 1 BOTTLE (71971-6030-5)
Product NDC	71971-6030
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Real Relief
Non-Proprietary Name	Allium Cepa, Aralia Racemosa, Arsenicum Album, Cuprum Metallicum, Euphrasia Officinalis, Nux Vomica, Sabadilla, Sticta Pulmonaria
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20200101
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Homeolab International (Canada) inc
Substance Name	ARALIA RACEMOSA ROOT; ARSENIC TRIOXIDE; COPPER; EUPHRASIA STRICTA; LOBARIA PULMONARIA; ONION; SCHOENOCAULON OFFICINALE SEED; STRYCHNOS NUX-VOMICA SEED
Strength	8; 8; 8; 8; 8; 8; 8; 8
Strength Unit	[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacy Classes	Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]