GELUSIL - aluminum hydroxide, dimethicone 410, magnesium hydroxide and silicon dioxide tablet, chewable 
WellSpring Pharmaceutical Corporation

----------

Gelusil Tablets

Drug Facts

Active ingredients (in each tablet)                  Purpose
Aluminum hydroxide dried gel 200 mg........................Antacid
Magnesium hydroxide 200 mg....................................Antacid
Simethicone 25 mg......................................................Antigas

Uses

Relieves:

• heartburn
• sour stomach
• acid indigestion
• bloating, pressure and discomfort commonly referred to as gas

Warnings

Do not use if you are presently taking a prescription antibiotic drug containing any form of tetracycline

Ask a doctor before use if you have

• kidney disease
• a magnesium restricted diet

Ask a doctor or pharmacist before use if

you are now taking a prescription drug.  Antacids may interact with certain prescription drugs.

Stop use and ask a doctor if

symproms last more than 2 weeks

Keep out of reach of children.

In case of overdose get medical help or contact a Poison Control Center right away 1.800.222.1222

Directions

• Chew 2 to 4 tablets.  Repeat hourly if symptoms return, or as directed by a physician.
• Do not take more than 12 tablets in a 24-hour period, or use the maximum dosage for more than 2 weeks, except under the advice and supervision of a physician

Other information

• each tablet contains: magnesium 95 mg
• store at 59º to 77º (15º to 25ºC)
• do not use if blister or printed Gelusil foil seal is broken
• see side panel for lot number and expiration date

Inactive ingredients

flavors, magnesium stearate, mannitol, sorbitol, and sugar

Questions?

call 1-866-337-4500

Distributed by:
WellSpring Pharmaceutical Corporation
SARASOTA, FL 34243 USA
©WellSpring 2010         Made in Canada

Package Label

Package Label for Blister Pack

GELUSIL  antacid and antigas   tablet, chewable

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 65197-300 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (ALUMINUM HYDROXIDE) ALUMINUM HYDROXIDE 200 mg DIMETHICONE 410 (DIMETHICONE) DIMETHICONE 410 24 mg MAGNESIUM HYDROXIDE (MAGNESIUM HYDROXIDE) MAGNESIUM HYDROXIDE 200 mg SILICON DIOXIDE (SILICON DIOXIDE) SILICON DIOXIDE 1 mg

Inactive Ingredients Ingredient Name Strength MANNITOL   RAW SUGAR   MAGNESIUM STEARATE   SORBITOL

Product Characteristics Color WHITE Score no score Shape ROUND Size 16mm Flavor PEPPERMINT Imprint Code PD;GELUSIL;034 Contains

Packaging # NDC Package Description Multilevel Packaging 1 65197-300-10 10 BLISTER PACK In 1 CARTON contains a BLISTER PACK 1 10 TABLET In 1 BLISTER PACK This package is contained within the CARTON (65197-300-10)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part331	09/24/2008

Labeler - WellSpring Pharmaceutical Corporation (110999054)

Establishment
Name	Address	ID/FEI	Operations
Trillium Health Care Manufacturing Inc.		255426306	ANALYSIS, MANUFACTURE

Establishment
Name	Address	ID/FEI	Operations
WellSpring Pharmaceutical Corporation		110999054	MANUFACTURE

Revised: 06/2010WellSpring Pharmaceutical Corporation