"48951-3206-7" National Drug Code (NDC)

NDC Code	48951-3206-7
Package Description	1 POWDER in 1 BOTTLE, GLASS (48951-3206-7)
Product NDC	48951-3206
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	ACTIVATED CHARCOAL; ANTIMONY TRISULFIDE; ARSENIC TRIOXIDE; AVENS EXTRACT; BLACK PEPPER; GENTIANA LUTEA ROOT; GINGER; MATRICARIA RECUTITA; WORMWOOD
Strength	2; 3; 6; 3; 3; 3; 3; 3; 3
Strength Unit	[hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
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]