ANTACID ANTIGAS MAXIMUM STRENGTH- aluminum hydroxide, magnesium hydroxide, simethicone liquid 
TARGET Corporation

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 ingredient (in each 10 mL)

Aluminum hydroxide (equiv. to dried gel USP) 800 mg

Magnesium Hydroxide 800 mg

Simethicone 80 mg

Purpose

Antacid

Antacid

Antacid

Uses

  • for the relief of
    • acid indigestion
    • heartburn
    • sour stomach
    • upset stomach associated with these symptoms
    • pressure and bloating commonly referred to as gas
    • overindulgence in food and drink

Warnings

Do not take

more than 60 mL in a 24-hour period or use the maximum dosage for more than 2 weeks except under the advice and supervision of a physican

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 more than 2 weeks.

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

 In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

  • shake well before using
  • mL = milliliter
  • do not take more than 60 mL in 24 hours or use the maximum dosage for more than 2 weeks
  • measure only with dosing cup provided. Do not use any other dosing device
  • keep dosing cup with product
  • adults and children12 years and older: take 10-20 mL as needed, between or after meals, at bedtime, or as directed by a doctor
  • children under 12 years of age: do not use

Other information

  • each 10 mL contains: magnesium 335 mg, sodium 10 mg
  • store between  20-25°C (68-77°F).Avoid freezing 

Inactive ingredients

benzyl alcohol, carboxymethylcellulose sodium, flavor, glycerin, microcrystalline cellulose, purified water, sodium carbonate, sorbitol, sucralose, xanthan gum

Questions or comments?

1-800-910-6874

Principal Display Panel

Compare to active ingredients in Mylanta® Maximum Strength*

Maximum Strength fast acting

antacid

anti-gas

aluminum hydroxide

magnesium hydroxide

simethicone

soothing relief of heartburn,

acid indigestion, sour stomach

sugar, paraben and alcohol free

*This product is not manufactured or distributed by McNeil Consumer Pharmaceuticals Co., distributor of Mylanta® Maximum Strength.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND OR UNDER CAP IS BROKEN OR MISSING.

Distributed by Target Corporation

Minneapolis, MN 55403

TM & ©2018 Target Brands, Inc.

Product Label

Aluminum hydroxide (equal to dried gel USP) 800 mg Magnesium hydroxide 800 mg Simethicone 80 mg

TARGET Maximum Strength Antacid anti-gas

ANTACID ANTIGAS  MAXIMUM STRENGTH
aluminum hydroxide, magnesium hydroxide, simethicone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-528
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE800 mg  in 10 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE800 mg  in 10 mL
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE80 mg  in 10 mL
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
GLYCERIN (UNII: PDC6A3C0OX)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
WATER (UNII: 059QF0KO0R)  
SODIUM CARBONATE (UNII: 45P3261C7T)  
SORBITOL (UNII: 506T60A25R)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-528-12355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/31/201812/30/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart33101/31/201812/30/2022
Labeler - TARGET Corporation (006961700)

Revised: 11/2020
Document Id: 149e9c19-de26-4de2-a6ab-f2121e617e6a
Set id: a0eccaf0-acde-4016-9515-5b4576908397
Version: 4
Effective Time: 20201109
 
TARGET Corporation