"48951-3257-4" National Drug Code (NDC)

NDC Code	48951-3257-4
Package Description	60 g in 1 BOTTLE, GLASS (48951-3257-4)
Product NDC	48951-3257
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Carbo Chamomilla
Non-Proprietary Name	Carbo Chamomilla
Dosage Form	POWDER
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc
Substance Name	ACORUS CALAMUS ROOT; ACTIVATED CHARCOAL; ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; BLACK PEPPER; GENTIANA LUTEA ROOT; GEUM URBANUM ROOT; GINGER; MATRICARIA RECUTITA; WORMWOOD
Strength	4; 2; 4; 6; 5; 3; 3; 3; 3; 3
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; [hp_X]/g; [hp_X]/g
Pharmacy Classes	Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]