SUNMARK ANTACID- aluminum hydroxide, magnesium hydroxide, simethicone liquid 
Mckesson

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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McKesson Antacid Drug Facts

Active ingredient (in each 5 mL teaspoon)

Aluminum hydroxide (equiv. to dried gel, USP) 200 mg

Magnesium hydroxide 200 mg

Simethicone 20 mg

Purpose

Antacid

Antigas

Uses

relieves

•
heartburn
•
acid indigestion
•
sour stomach
•
upset stomach due to these symptoms
•
pressure and bloating 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.

When using this product

do not exceed 24 teaspoonsfuls (120 mL) in a 24-hour period, or use the maximum dosage for more than 2 weeks, unless directed by a doctor

Keep out of reach of children.

Directions

•
shake well
•
adults and children 12 years and older: take 2-4 teaspoonsfuls (10-20 mL) between meals, at bedtime, or as directed by a doctor
•
children under 12 years: ask a doctor

Other information

•
each teaspoon contains: magnesium 85 mg
•
does not meet USP requirements for preservative effectiveness
•
store at 20°-25°C (68º-77ºF)

Inactive ingredients

butylparaben, flavor, hypromellose, microcrystalline cellulose and carboxymethylcellulose sodium, peppermint oil, propylparaben, purified water, simethicone emulsion, sorbitol, sorbitol solution

Questions or comments?

1-800-719-9260

Principal Display Panel

COMPARE TO MYLANTA® REGULAR STRENGTH ACTIVE INGREDIENTS

antacid

Regular Strength

Antacid/Anti-Gas

Fast relief of

heartburn, acid indigestion, & sour stomach

CLASSIC ORIGINAL FLAVOR

ALCOHOL 0.2%

GLUTEN FREE

Antacid Front Label
Antacid Back Label
SUNMARK ANTACID 
aluminum hydroxide, magnesium hydroxide, simethicone liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-020
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE200 mg  in 5 mL
MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE200 mg  in 5 mL
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE20 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
BUTYLPARABEN (UNII: 3QPI1U3FV8)  
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SORBITOL (UNII: 506T60A25R)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
Product Characteristics
ColorWHITE (opaque) Score    
ShapeSize
FlavorMINT (lemon, original) Imprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-020-39355 mL in 1 BOTTLE; Type 0: Not a Combination Product08/21/200304/14/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33108/21/200304/14/2018
Labeler - Mckesson (177667227)

Revised: 4/2018
Document Id: 48c1ca9b-45f5-4719-8d8d-639274991339
Set id: f59bee90-8fd3-45ef-8a5d-5ea7aece7cb3
Version: 3
Effective Time: 20180406
 
Mckesson