"48951-8111-1" National Drug Code (NDC)

NDC Code	48951-8111-1
Package Description	10 AMPULE in 1 BOX (48951-8111-1) > 1 mL in 1 AMPULE
Product NDC	48951-8111
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Quartz Oxalis Nicotiana
Non-Proprietary Name	Quartz Oxalis Nicotiana
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	OXALIS ACETOSELLA LEAF; SILICON DIOXIDE; SILVER; TOBACCO LEAF
Strength	30; 30; 30; 30
Strength Unit	[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 Plant Allergenic Extract [EPC], Plant Proteins [CS]