ANTACID- calcium carbonate tablet, chewable 
Major Pharmaceuticals

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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Major Pharmaceuticals Antacid Tablets Drug Facts

Active ingredient (in each tablet)

Calcium carbonate USP 500mg

Purpose

Antacid

Uses

relieves

•
heartburn
•
sour stomach
•
acid indigestion
•
upset stomach associated with these symptoms

Warnings

Ask a doctor before use if you have

•
kidney stones
•
a calcium-restricted diet

Ask a doctor or pharmacist before use if you are

•
now taking a prescription drug. Antacids may interact with certain prescription drugs.

When using this product

•
do not take more than 15 tablets in 24 hours
•
do not use the maximum dosage for more than 2 weeks

Keep out of reach of children.

Directions

•
chew 2 - 4 tablets as symptoms occur, or as directed by a doctor

Other information

•
each tablet contains: calcium 215 mg and magnesium 5 mg
•
store at 20-25°C (68-77°F)

Inactive ingredients

dextrose, flavor, maltodextrin, mineral oil, polyethylene glycol, powdered cellulose, talc

Questions?

1-800-616-2471

Principal Display Panel

COMPARE TO the active ingredient of TUMS®

CALCIUM

Antacid Tablets

Regular Strength

ANTACID/CALCIUM SUPPLEMENT

Calcium Carbonate 500 mg

Peppermint

Naturally & Artificially Flavored

DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING

Antacid Tablets Front Label

Antacid Tablets Front Label

Antacid Tablets Back Label

Antacid Tablets Front Label

Antacid Tablets Back Label

ANTACID 
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0904-1257
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE500 mg
Inactive Ingredients
Ingredient NameStrength
DEXTROSE (UNII: IY9XDZ35W2)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
MINERAL OIL (UNII: T5L8T28FGP)  
POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize17mm
FlavorPEPPERMINTImprint Code L485
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0904-1257-92150 in 1 BOTTLE; Type 0: Not a Combination Product10/30/199206/08/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33110/30/199206/08/2013
Labeler - Major Pharmaceuticals (191427277)

Revised: 11/2017
Document Id: 5f52e3e5-cefe-4308-b098-b244b2476e31
Set id: fdc21244-229a-47e4-8590-7803a4845c61
Version: 2
Effective Time: 20171125
 
Major Pharmaceuticals