"48951-2077-1" National Drug Code (NDC)

NDC Code	48951-2077-1
Package Description	10 AMPULE in 1 BOX (48951-2077-1) > 1 mL in 1 AMPULE
Product NDC	48951-2077
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Borago Nicotiana
Non-Proprietary Name	Borago Nicotiana
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ALUMINUM OXIDE; BORAGE; CENTAUREA BENEDICTA; FERROUS ARSENATE; HAMAMELIS VIRGINIANA LEAF; HORSE CHESTNUT; TOBACCO LEAF
Strength	8; 3; 3; 10; 3; 10; 6
Strength Unit	[hp_X]/mL; [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 Plant Allergenic Extract [EPC], Plant Proteins [CS]