"48951-8307-4" National Drug Code (NDC)

NDC Code	48951-8307-4
Package Description	50 g in 1 BOTTLE, GLASS (48951-8307-4)
Product NDC	48951-8307
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Bismuth Magnesite Comp.
Non-Proprietary Name	Bismuth Magnesite Comp.
Dosage Form	POWDER
Usage	ORAL
Start Marketing Date	20090109
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	ANTIMONY TRISULFIDE; BISMUTH; CORALLIUM RUBRUM EXOSKELETON; MAGNESITE; POTASSIUM ACETATE; SAFFRON
Strength	6; 3; 6; 3; 6; 6
Strength Unit	[hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
Pharmacy Classes	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]