"48951-3040-5" National Drug Code (NDC)

NDC Code	48951-3040-5
Package Description	60 g in 1 TUBE (48951-3040-5)
Product NDC	48951-3040
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Cartilago Betula
Non-Proprietary Name	Cartilago Betula
Dosage Form	CREAM
Usage	TOPICAL
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; 3; 6; 7; 10; 3; 8
Strength Unit	[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
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]