"48951-3039-1" National Drug Code (NDC)

NDC Code	48951-3039-1
Package Description	10 AMPULE in 1 BOX (48951-3039-1) / 1 mL in 1 AMPULE
Product NDC	48951-3039
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Cartilago Betula
Non-Proprietary Name	Cartilago Betula
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ACONITUM NAPELLUS; ARNICA MONTANA; BETULA PUBESCENS LEAF; BOS TAURUS CARTILAGE; FORMICA RUFA; GOLD; ONION; TIN
Strength	6; 6; 5; 8; 17; 10; 17; 8
Strength Unit	[hp_X]/mL; [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], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS]