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

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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:

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

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

Other information

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

Package Label for Blister Pack

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: 06/2010 WellSpring Pharmaceutical Corporation