HEARTBURN RELIEF- aluminum hydroxide and magnesium carbonate suspension 
CHAIN DRUG MARKETING ASSOCIATION

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QC 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 (1-800-222-1222) 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

1

HEARTBURN RELIEF 
aluminum hydroxide and magnesium carbonate suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-565
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
Color    Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63868-565-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00111/01/2019
Labeler - CHAIN DRUG MARKETING ASSOCIATION (011920774)
Registrant - GCP Laboratories (965480861)
Establishment
NameAddressID/FEIBusiness Operations
GCP Laboratories965480861manufacture(63868-565)

Revised: 11/2023
Document Id: 097f7264-6848-61fb-e063-6294a90a3f2f
Set id: b4656a2f-a866-5f7a-e053-2995a90ac2c2
Version: 2
Effective Time: 20231106
 
CHAIN DRUG MARKETING ASSOCIATION