ANTACID ANTIGAS MAXIMUM STRENGTH- aluminum hydroxide, magnesium hydroxide, dimethicone suspension 
Chain Drug Consortium, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients

Aluminum hydroxide(equivalent to Dried Gel, USP) 400 mg
Magnesium hydroxide 400 mg
Simethicone 40 mg

Purpose

Antacid
Antigas

Uses

relieves: • heartburn • sour stomach • acid indigestion
• upset stomach due to these symptoms • symptoms of 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

presently taking a prescription drug. Antacids may interact with certain
prescription drugs

Stop use and ask a doctor

if symptoms last for more
than 2 weeks

If pregnant or breast-feeding

ask a health professional before use.

Keep this and all drugs out of the reach of children.

In case of accidental overdose, seek professional assistance
or contact a Poison Control Center immediately.

Other information

store at room temperature tightly closed

do not freeze

each teaspoon contains:

potassium 2 mg, magnesium 167 mg

Inactive ingredients

benzyl alcohol,
flavors, glycerin, hydroxyethyl cellulose,
potassium citrate, propylene glycol,
purified water, sorbitol

Directions

Package Label

 Aluminum hydroxide 400 mg, Magnesium hydroxide 400 mg, Dimethicone 40 mg

Antacid Antigas Maximum Strength

ANTACID ANTIGAS MAXIMUM STRENGTH 
aluminum hydroxide, magnesium hydroxide, dimethicone suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-050
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE400 mg  in 5 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE400 mg  in 5 mL
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE40 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SORBITOL (UNII: 506T60A25R)  
Product Characteristics
Color    Score    
ShapeSize
FlavorLEMON (Lemon) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-050-12355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33106/03/2009
Labeler - Chain Drug Consortium, LLC (101668460)

Revised: 2/2016
Document Id: f749802f-8258-4410-9781-8385ebc1c397
Set id: 0d353525-ae3f-43c3-a5fd-56b885c06f47
Version: 6
Effective Time: 20160204
 
Chain Drug Consortium, LLC