OTC Medication Information: Calcium Antacid

CALCIUM ANTACID — 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.

Active ingredient (in each tablet)

Calcium carbonate 500 mg

Purpose

Antacid

Uses

relieves

  • acid indigestion
  • heartburn

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

  • chew 2-4 tablets as symptoms occur, or as directed by a doctor.
Other information
  • do not use if printed seal under the cap is torn or missing.
  • store at room temperature.

Inactive ingredients

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

Principal Display Panel

Sunmark

COMPARE TO TUMSĀ® ACTIVE INGREDIENT

calcium anatcid

Regular Strength

Fast relief of heartburn and acid indigestion

Daily source of calcium

PEPPERMINT FLAVOR

Calcium antacid front label
(click image for full-size original)
Calcium antacid back label
(click image for full-size original)

CALCIUM ANTACID
calcium antacid tablet, chewable
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:49348-957
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM CARBONATE (CALCIUM CATION and CARBONATE ION) CALCIUM CARBONATE 500 mg
Inactive Ingredients
Ingredient Name Strength
STARCH, CORN
CROSPOVIDONE
DEXTROSE
MAGNESIUM STEARATE
MALTODEXTRIN
SUCROSE
TALC
Product Characteristics
Color white Score no score
Shape ROUND Size 16mm
Flavor PEPPERMINT Imprint Code GDC113
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:49348-957-21 150 TABLET, CHEWABLE (TABLET) in 1 BOTTLE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part331 03/05/2011
Labeler — McKesson (177667227)

Revised: 01/2012 McKesson

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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