GELUSIL- alumina, magnesia, simethicone tablet, chewable

Gelusil by

Drug Labeling and Warnings

Gelusil by is a Otc medication manufactured, distributed, or labeled by WellSpring Pharmaceutical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients (in each tablet)  

Aluminum hydroxide dried gel 200 mg
Magnesium hydroxide 200 mg
Simethicone 25 mg

Purpose

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

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

symptoms 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

If pregnant or breastfeeding

 ask a health professional before use.

Directions

• For adults and children 12 years of age and older: Chew 2 to 4 tablets.  Repeat hourly if symptoms return, or as directed by a physician
• Children under 12: ask a doctor
• 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 below 30°C (86°F)
• Tamper Evident. Do not use if blister or printed Gelusil foil seal is broken
• See end panel for lot number and expiration date

Inactive ingredients

Dextrose, flavors, magnesium stearate, maltodextrin, microcrystalline cellulose, silica, sucralose

Questions?

Call 1-844-241-5454 Money Back Guarantee

SPL UNCLASSIFIED SECTION

© WellSpring 2018
Sarasota, FL 34243 USA
Made in USA

Principal display panel - Carton

 

INGREDIENTS AND APPEARANCE

GELUSIL 
alumina, magnesia, simethicone tablet, chewable

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0)	ALUMINUM HYDROXIDE	200 mg
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838)	MAGNESIUM HYDROXIDE	200 mg
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	24 mg
SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4)	SILICON DIOXIDE	1 mg

Inactive Ingredients
Ingredient Name	Strength
DEXTROSE (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SILICON (UNII: Z4152N8IUI)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65197-300-10	10 in 1 CARTON	09/24/2008
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2	NDC: 65197-300-11	100 in 1 BOTTLE; Type 0: Not a Combination Product	12/01/2018

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)