"48951-8175-2" National Drug Code (NDC)

NDC Code	48951-8175-2
Package Description	1350 PELLET in 1 BOTTLE, GLASS (48951-8175-2)
Product NDC	48951-8175
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Secale Betula
Non-Proprietary Name	Secale Betula
Dosage Form	PELLET
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ARNICA MONTANA; BETULA PUBESCENS BARK; BETULA PUBESCENS LEAF; BOS TAURUS EYE; CLAVICEPS PURPUREA SCLEROTIUM; LEAD SULFIDE; LEVISTICUM OFFICINALE ROOT; TOBACCO LEAF
Strength	12; 4; 3; 8; 6; 8; 6; 6
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], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Iron [CS], Non-Standardized Plant Allergenic Extract [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Plant Proteins [CS]