"0135-0096-26" National Drug Code (NDC)

NDC Code	0135-0096-26
Package Description	100 TABLET, CHEWABLE in 1 BOTTLE (0135-0096-26)
Product NDC	0135-0096
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Gaviscon
Proprietary Name Suffix	Regular Strength
Non-Proprietary Name	Aluminum Hydroxide And Magnesium Trisilicate
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20110613
Marketing Category Name	NDA
Application Number	NDA018685
Manufacturer	GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Substance Name	ALUMINUM HYDROXIDE; MAGNESIUM TRISILICATE
Strength	80; 14.2
Strength Unit	mg/1; mg/1
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]