"71399-0051-2" National Drug Code (NDC)

NDC Code	71399-0051-2
Package Description	12 BOTTLE in 1 PACKAGE (71399-0051-2) / 296 mL in 1 BOTTLE
Product NDC	71399-0051
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Onelax
Proprietary Name Suffix	Saline Laxative
Non-Proprietary Name	Magnesium Citrate
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20230804
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M007
Manufacturer	AKRON PHARMA INC
Substance Name	MAGNESIUM CITRATE
Strength	1.745
Strength Unit	g/29.6mL
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]