GERI-LANTA MAXIMUM STRENGTH

Product NDC

68788-4189

11-digit product format

687884189

Labeler code

68788

Product ID

68788-4189_3b049027-30ac-4c78-a4f1-8191f7ed45bf

Type

HUMAN OTC DRUG

Nonproprietary name

aluminum hydroxide, magnesium hydroxide, dimethicone

Dosage form

SUSPENSION

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

M001

Marketing category

OTC MONOGRAPH DRUG

Marketing start

2000-01-01

Substance

ALUMINUM HYDROXIDE; MAGNESIUM HYDROXIDE; DIMETHICONE, UNSPECIFIED

Active strength

400; 400; 40 mg/5mL; mg/5mL; mg/5mL

Pharmacologic 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], Skin Barrier Activity [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

NDC exclude flag

No

Listing certified through

2027-12-31

Current FDA listing

Yes