ALKA-SELTZER HEARTBURN RELIEF PEPPERMINT- calcium carbonate gum, chewing 
Bayer HealthCare LLC.

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Alka-Seltzer Heartburn Relief Gum (peppermint), UI 1614661

Drug Facts

Active ingredient (in each chewing piece)

Calcium carbonate 750 mg

Purpose

Antacid

Uses

Uses for the relief of:

● acid indigestion ● heartburn ● sour stomach

● upset stomach associated with these symptoms

Warnings

Do not use if you have ever had an allergic reaction to this product or any of its ingredients

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

When using this product
● do not use more than 5 pieces in a 24-hour period

● if pregnant, do not use more than 5 pieces in a 24-hour period

● do not use the maximum dosage of this product for more

than 2 weeks except under the advice and supervision of a

physician

If pregnant or breast-feeding, inform your doctor that you are using this product.

Keep out of reach of children.

Directions

Directions

● adults and children 12 years and over: chew 1 - 2 pieces as symptoms occur or as directed by a doctor

● children under 12 years: consult a doctor

● do not use more than 5 pieces in a 24-hour period

● if pregnant, do not use more than 5 pieces in a 24-hour period

● do not swallow the gum

Other information

Other information

● each piece contains: calcium 300 mg

● store at room temperature. Avoid humidity and excessive heat above 40ºC (104ºF).

Inactive ingredients acesulfame potassium, butylated hydroxytoluene, copovidone, FD&C Blue No.1 Aluminum Lake, flavors, gum base, isomalt, magnesium stearate, sorbitol, sucralose, talc, titanium dioxide

Questions or comments? 1-800-986-0369

(Mon – Fri 9AM – 5PM EST)

Carton 16 count

Works Fast!

Alka-Seltzer®

Calcium Carbonate/Antacid

EXTRA STRENGTH

HEARTBURN RELIEF

GUM

peppermint

16 Pieces

16 count carton

ALKA-SELTZER HEARTBURN RELIEF  PEPPERMINT
calcium carbonate gum, chewing
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0280-0002
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 mg
Inactive Ingredients
Ingredient NameStrength
TALC (UNII: 7SEV7J4R1U)  
COPOVIDONE K25-31 (UNII: D9C330MD8B)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
ISOMALT (UNII: S870P55O2W)  
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
FD&C BLUE NO. 1--ALUMINUM LAKE (UNII: J9EQA3S2JM)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
SORBITOL (UNII: 506T60A25R)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
Colorblue (Blue and Blue; Active on imprint side) Scoreno score
ShapeROUNDSize16mm
FlavorPEPPERMINTImprint Code 750
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0280-0002-012 in 1 CARTON03/02/2020
18 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00103/02/2020
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 12/2023
Document Id: 0bb54312-8ca7-15e8-e063-6294a90a2b31
Set id: 9b8e802f-91b6-4559-e053-2a95a90aff67
Version: 6
Effective Time: 20231204
 
Bayer HealthCare LLC.