"48951-8125-3" National Drug Code (NDC)

NDC Code	48951-8125-3
Package Description	60 mL in 1 BOTTLE, DROPPER (48951-8125-3)
Product NDC	48951-8125
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Renes Betula
Non-Proprietary Name	Renes Betula
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ARCTOSTAPHYLOS UVA-URSI LEAF; BETULA PUBESCENS LEAF; CAPSELLA BURSA-PASTORIS; COPPER; CYTISUS SCOPARIUS FLOWERING TOP; ELYMUS REPENS ROOT; EQUISETUM ARVENSE TOP; ONONIS REPENS ROOT; PARSLEY; PETROSELINUM CRISPUM ROOT; PORK KIDNEY; SOLIDAGO VIRGAUREA FLOWERING TOP
Strength	2; 4; 2; 8; 3; 4; 3; 2; 2; 2; 6; 2
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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], Vegetable Proteins [CS]