"71971-9066-8" National Drug Code (NDC)

NDC Code	71971-9066-8
Package Description	1 BOTTLE in 1 CARTON (71971-9066-8) > 25 mL in 1 BOTTLE
Product NDC	71971-9066
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Kids Relief
Non-Proprietary Name	Pulsatilla, Allium Cepa, Arsenicum Album, Nux Vomica, Euphrasia Offinalis, Sabadilla, Aralia Racemosa, Cuprum Metallicum
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20190726
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Homeolab International (Canada) inc
Substance Name	ANEMONE PULSATILLA; ARALIA RACEMOSA ROOT; ARSENIC TRIOXIDE; COPPER; EUPHRASIA STRICTA; ONION; SCHOENOCAULON OFFICINALE SEED; STRYCHNOS NUX-VOMICA SEED
Strength	8; 6; 8; 8; 6; 6; 6; 6
Strength Unit	[hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL; [hp_X]/25mL
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]