ANTACID RELIEF- calcium carbonate tablet, chewable 
Safeway

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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Regular Strength Antacid Relief Peppermint Tablets

Active ingredient (in each tablet)

Calcium carbonate 500 mg

Purpose

Antacid

Uses

relieves

Warnings

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 15 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

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

Keep out of reach of children.

Directions

Other information

Inactive ingredients

corn starch, crospovidone, dextrose, flavor, magnesium stearate, maltodextrin, sucrose, talc

Principal Display Panel

COMPARE TO TUMS® active ingredient* 

Signature Care

Regular Strength Anatcid Relief Tablets

CALCIUM CARBONATE 500 mg

PEPPERMINT FLAVOR

150 Tablets

image description

ANTACID RELIEF 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-913
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE500 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
CROSPOVIDONE (UNII: 2S7830E561)  
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
SUCROSE (UNII: C151H8M554)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize16mm
FlavorPEPPERMINTImprint Code GDC113
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21130-913-17150 in 1 BOTTLE; Type 0: Not a Combination Product08/08/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33108/08/2015
Labeler - Safeway (009137209)

Revised: 1/2022
Document Id: 43a6b203-8c4c-40ef-9717-89f464af6ba6
Set id: 8b2c533b-6ae8-445d-840c-9ad25e8fd1fd
Version: 4
Effective Time: 20220112
 
Safeway