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Miralac

Medically reviewed by Drugs.com. Last updated on Jan 19, 2020.

Dosage form: tablet
Ingredients: CALCIUM CARBONATE 420mg
Labeler: Honeywell Safety Products USA, Inc
NDC Code: 0498-0303

Miralac

Active ingredient (in each chewable tablet)

Calcium carbonate 420 mg

Purpose

Antacid

Uses

for the relief of

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

Warnings


Ask a doctor before use if you have
  • kidney stones
  • calcium-restricted diet

Ask a doctor before use if you are

presently taking a prescription drug. Antacids may interfere with certain prescription drugs

When using this product

do not take more than 12 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 the reach of children.

In case of accidental overdose, seek professional assistance or contact a Poison Control Center immediately.

Directions

chew 1 to 2 tablets every 4 hours as symptoms occur, or as directed by a doctor.

Other information
  • each tablet contains: calcium 170 mg
  • sucrose free
  • lactose free
  • store at room temperature
  • TAMPER EVIDENT PACKETS- DO NOT USE IF OPEN OR TORN





Inactive ingredients

magnesium stearate, mint flavor, silicon dioxide, sorbitol, starch

Questions or comments?

1-800-430-5490

Principal Display Panel

MIRALAC 
calcium carbonate tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0303
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CALCIUM CARBONATE (CALCIUM CATION and CARBONATE ION) CALCIUM CARBONATE420 mg
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM STEARATE 
SILICON DIOXIDE 
SORBITOL 
STARCH, CORN 
Product Characteristics
Colorwhite (White) Score2 pieces
ShapeROUNDSize11mm
FlavorMINT (Mint Flavor) Imprint CodeFR8
Contains    
Packaging
#Item CodePackage Description
1NDC:0498-0303-10100 PACKET in 1 BOX, UNIT-DOSE
12 TABLET in 1 PACKET
2NDC:0498-0303-25250 PACKET in 1 BOX, UNIT-DOSE
22 TABLET in 1 PACKET
3NDC:0498-0303-50500 BOX, UNIT-DOSE in 1 BOX, UNIT-DOSE
32 TABLET in 1 BOX, UNIT-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart33102/22/2012
Labeler - Honeywell Safety Products USA, Inc (079287321)
Registrant - Honeywell Safety Products USA, Inc (079287321)
Establishment
NameAddressID/FEIOperations
Honeywell Safety Products USA, Inc079287321repack(0498-0303)

 
Honeywell Safety Products USA, Inc

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.