ANTACID- calcium carbonate tablet, chewable 
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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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Select Brand Antacid Tablets Regular Strength Peppermint

Active ingredient (in each tablet)

Calcium carbonate 500 mg

Purpose

Antacid

Uses

relieves

Warnings

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

do not take more than 16 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.

Keep out of reach of children.

Directions

Other information

Inactive ingredients

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

Principal Display Panel

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Anatcid Tablets

Regular Strength

Peppermint

COMPARE TO ACTIVE INGREDIENT IN TUMS®

150 Chewable Tablets

Naturally and Artificially Flavored

label

ANTACID 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15127-210
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: 68401960MK)  
DEXTROSE (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:15127-210-24150 in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33112/12/2008
Labeler - Select Brand (043562370)

Revised: 8/2014
Document Id: 520d029a-5b8a-4bfe-9ef4-c7eb378cb4c2
Set id: 91b33a34-33eb-46a7-bb23-b3b3256b8205
Version: 1
Effective Time: 20140829
 
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