"48951-2131-1" National Drug Code (NDC)

NDC Code	48951-2131-1
Package Description	10 AMPULE in 1 BOX (48951-2131-1) > 1 mL in 1 AMPULE
Product NDC	48951-2131
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Berberis Populus
Non-Proprietary Name	Berberis Populus
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	BERBERIS VULGARIS ROOT BARK; LARIX DECIDUA RESIN; POPULUS TREMULOIDES POLLEN; SAW PALMETTO; URTICA URENS; WHITE PEPPER
Strength	2; 8; 3; 3; 3; 17
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacy Classes	Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS]