"48951-8099-3" National Drug Code (NDC)

NDC Code	48951-8099-3
Package Description	60 mL in 1 BOTTLE, DROPPER (48951-8099-3)
Product NDC	48951-8099
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Pulsatilla Tormentilla
Non-Proprietary Name	Pulsatilla Tormentilla
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090901
Marketing Category Name	UNAPPROVED HOMEOPATHIC
Manufacturer	Uriel Pharmacy Inc.
Substance Name	MAGNESIUM HYDROXIDE; MAMMAL LIVER; POTENTILLA ERECTA ROOT; PULSATILLA VULGARIS
Strength	4; 4; 30; 12
Strength Unit	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacy Classes	Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]