"48951-7080-1" National Drug Code (NDC)

NDC Code	48951-7080-1
Package Description	10 AMPULE in 1 BOX (48951-7080-1) > 1 mL in 1 AMPULE
Product NDC	48951-7080
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Nux Vomica Chamomilla
Non-Proprietary Name	Nux Vomica Chamomilla
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ACTIVATED CHARCOAL; MATRICARIA RECUTITA; PORK KIDNEY; ROBINIA PSEUDOACACIA BARK; STRYCHNOS NUX-VOMICA SEED; TOBACCO LEAF
Strength	20; 3; 7; 6; 8; 10
Strength Unit	[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], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS]