MedPath

GELUSIL EXTRA STRENGTH LIQ

GELUSIL EXTRA STRENGTH LIQ

Discontinued
DIN Number

01945858

Drug Class

Human

Market Date

Dec 31, 1992

Company
HC

warner-lambert canada inc.

Product Information

Detailed information about this Health Canada approved drug product, including dosage form, route of administration, and regulatory classification.

Product Details

Health Canada regulatory and product classification information

Regulatory Identifiers
DIN Number01945858
AIG Number0201452013
Classification & Schedule
C
Drug Class
Human
S
Schedule
OTC
A
ATC Code
A02AD01 ORDINARY SALT COMBINATIONS
Product Specifications
Dosage FormLiquid
Route of AdministrationOral
AHFS Classification56:04.00
Health Canada Classification

ACTIVE INGREDIENTS (2)

ALUMINUM HYDROXIDEActive
Strength: 650 MG / 5 ML
Monograph: ALUMINUM HYDROXIDE
MAGNESIUM HYDROXIDEActive
Strength: 350 MG / 5 ML
Monograph: MAGNESIUM HYDROXIDE

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.