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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Extra Strength Antacid Relief Tablets

Active ingredient (in each tablet)

Calcium carbonate 1000 mg

Purpose

Antacid

Uses

relieves: acid indigestion, heartburn

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 7 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.

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

Directions

Other information

Inactive ingredients

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

PDP

Compare to the TUMS Ultra strength active ingredient

Ultra strength

Antacid Relief Tablets

Calcium Carbonate 1000 mg

Peppermint Flavor

Chewable

Rich in calcium

Relief of: acid indigestion/heartburn

72 tablets

LBL

ANTACID RELIEF 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-472
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION1000 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
ShapeROUNDSize17mm
FlavorPEPPERMINTImprint Code G171
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:21130-472-6872 in 1 BOTTLE; Type 0: Not a Combination Product11/11/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33111/11/2015
Labeler - Safeway (009137209)
Establishment
NameAddressID/FEIBusiness Operations
Guardian Drug Company119210276manufacture(21130-472)

Revised: 1/2016
Document Id: 60f1fdff-c294-47b8-a67f-211f5cd8b3e3
Set id: ead5101d-761a-4d1d-b14b-4dd548d2def6
Version: 2
Effective Time: 20160122
 
Safeway