SUNMARK CALCIUM ANTACID REGULAR STRENGTH- calcium carbonate tablet, chewable 
McKesson

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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McKesson Calcium Antacid Drug Facts

Active ingredient (in each tablet)

Calcium carbonate 500 mg

Purpose

Antacid

Uses

relieves

•
heartburn
•
sour stomach
•
acid indigestion

Warnings

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 exceed 15 tablets daily or use the maximum dosage for more than 2 weeks

Keep out of reach of children.

Directions

chew 2 to 4 tablets as symptoms occur

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

Principal Display Panel

Compare to Tums® Active Ingredient

Calcium Antacid

Regular Strength

Chewable

Antacid & Calcium Supplement

500 mg Calcium Carbonate

Naturally Flavored

Peppermint

Calcium Antacid Front Label

Calcium Antacid Front Label

Calcium Antacid Back Label

Calcium Antacid Front Label

Calcium Antacid Back Label

SUNMARK CALCIUM ANTACID  REGULAR STRENGTH
calcium carbonate tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-169
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)  
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize17mm
FlavorPEPPERMINTImprint Code L485
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49348-169-21150 in 1 BOTTLE; Type 0: Not a Combination Product08/18/200309/13/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33108/18/200309/13/2012
Labeler - McKesson (177667227)

Revised: 11/2017
Document Id: 705dddba-0952-4f9f-9de5-e6ad97b3434f
Set id: 7418e4e8-d8c9-48bf-aa0c-016641edec8c
Version: 2
Effective Time: 20171117
 
McKesson