EXTRA STRENGTH HEARTBURN RELIEF- aluminum hydroxide and magnesium carbonate suspension 
CVS PHARMACY,INC.

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CVS ES heartburn relief

Active ingredients (in each 5 mL teaspoonful)

Aluminum hydroxide 254 mg
Magnesium carbonate 237.5 mg

Purpose

Antacid

Uses

relieves

Warnings

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

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 right away

Directions

Other information

Inactive ingredients

benzyl alcohol, edetate disodium, flavor, glycerin, purified water, saccharin sodium, simethicone emulsion, sodium alginate, sorbitol solution, xanthan gum

Questions or comments?

1-800-540-3765

package Label

CVS health

Compare to the active
ingredients in Gaviscon®*

EXTRA STRENGTH

Heartburn Relief

ALUMINA AND MAGNESIUM
CARBONATE ORAL SUSPENSION USP

ANTACID

Cherry Flavor

12 FL OZ (355 mL)

cvs618

EXTRA STRENGTH HEARTBURN RELIEF 
aluminum hydroxide and magnesium carbonate suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-628
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE254 mg  in 5 mL
MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE237.5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
SORBITOL (UNII: 506T60A25R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69842-628-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00102/01/2017
Labeler - CVS PHARMACY,INC. (062312574)
Registrant - GCP Laboratories (965480861)
Establishment
NameAddressID/FEIBusiness Operations
GCP Laboratories965480861manufacture(69842-628)

Revised: 10/2023
Document Id: 09079688-4a35-fb60-e063-6394a90ae488
Set id: 53fc327e-e345-26f2-e054-00144ff8d46c
Version: 2
Effective Time: 20231031
 
CVS PHARMACY,INC.