ALKA-SELTZER HEARTBURN RELIEFCHEWS- calcium carbonate tablet, chewable 
Bayer HealthCare LLC.

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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Alka-Seltzer ® Heartburn ReliefChews™

Drug Facts

Active ingredient (in each chewable tablet)

Calcium carbonate 750 mg

Purpose

Antacid

Uses

for the relief of:

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 take more than 10 chewable tablets 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
  • constipation may occur

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children.

Directions

Other information

Inactive ingredients

acacia, beeswax, carmine, carnauba wax, citric acid, corn starch, corn syrup, DL-alpha tocopherol, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #5 lake (tartrazine), FD&C yellow #6, FD&C yellow #6 aluminum lake, FD&C yellow #6 lake, flavors, hydrogenated coconut oil, medium chain triglycerides, methyl paraben, modified starch, phosphoric acid, pregelatinized modified starch, propyl paraben, propylene glycol, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide

Questions?

1-800-986-0369 (Mon – Fri 9AM – 5PM EST) or www.alkaseltzer.com

Dist. by:
Bayer HealthCare LLC
Whippany, NJ 07981

PRINCIPAL DISPLAY PANEL - 36 Tablet Bottle Label

assorted fruit

Alka-

Seltzer
®

Calcium Carbonate /

Antacid

EXTRA STRENGTH

HEARTBURN

RELIEFCHEWS™

Fast Powerful Relief

36 CHEWABLE TABLETS

Label 36 count

ALKA-SELTZER HEARTBURN RELIEFCHEWS 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0280-0221
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
YELLOW WAX (UNII: 2ZA36H0S2V)  
ACACIA (UNII: 5C5403N26O)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
STARCH, CORN (UNII: O8232NY3SJ)  
CORN SYRUP (UNII: 9G5L16BK6N)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SHELLAC (UNII: 46N107B71O)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SORBIC ACID (UNII: X045WJ989B)  
SORBITOL (UNII: 506T60A25R)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
SUCROSE (UNII: C151H8M554)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Coloryellow, orange, pinkScoreno score
ShapeROUNDSize18mm
FlavorLEMON, ORANGE, STRAWBERRYImprint Code AS
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0280-0221-3636 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/2014
2NDC:0280-0221-6060 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/2014
3NDC:0280-0221-12120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/15/2014
4NDC:0280-0221-9090 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/12/2015
5NDC:0280-0221-088 in 1 POUCH; Type 0: Not a Combination Product03/23/2016
6NDC:0280-0221-0132 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2020
7NDC:0280-0221-0266 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2020
8NDC:0280-0221-03200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33103/15/2014
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 8/2023
Document Id: 02f8f5fa-ed93-c5be-e063-6294a90a5484
Set id: bdb43d3b-ddcd-4359-a174-a5556e7c5f57
Version: 7
Effective Time: 20230815
 
Bayer HealthCare LLC.