"48951-8235-2" National Drug Code (NDC)

NDC Code	48951-8235-2
Package Description	1350 PELLET in 1 BOTTLE, GLASS (48951-8235-2)
Product NDC	48951-8235
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Renes Betula Special Order
Non-Proprietary Name	Renes Betula Special Order
Dosage Form	PELLET
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 TOP; EQUISETUM ARVENSE TOP; ONONIS REPENS ROOT; PARSLEY; PORK KIDNEY; SOLIDAGO VIRGAUREA FLOWERING TOP
Strength	3; 4; 3; 9; 4; 3; 4; 3; 3; 4; 3
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; [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], Vegetable Proteins [CS]