TUMS - calcium carbonate tablet 
GlaxoSmithKline Consumer Heathcare LP

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Drug Facts

Active ingredient (per tablet)

Calcium carbonate USP 500 mg

Purpose

Antacid

Uses relieves

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

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 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

• for calcium content see Supplement Facts
• store below 30oC (86oF)

 

Safety sealed- Do not use if printed inner seal beneath cap is missing or broken.

Calcium Supplement

USES: As a daily source of extra calcium.

DIRECTIONS: Chew 2 tablets twice daily with a meal.

Supplement Facts

Serving Size: 2 Tablets

Servings Per Container: 75

Amount Per Serving	%Daily Value
Calories 5
Sugars 1g
Calcium 400mg	40%

Inactive ingredients (assorted fruit)

sucrose, calcium carbonate, corn starch, talc, mineral oil, natural and artificial flavors, adipic acid, sodium polyphosphate, red 40 lake, yellow 6 lake, yellow 5 (tartrazine) lake, blue 1 lake

Inactive ingredient (peppermint)

sucrose, calcium carbonate, corn starch, talc, mineral oil, natural flavor, sodium polyphosphate

Questions?

1-800-897-7535

weekdays

www.tums.com

GlaxoSmithKline

Moon Twp, PA 15108

©2009 GSK

Principal Display Panel

TUMS®

CALCIUM RICH

ANTACID/CALCIUM SUPPLEMENT

REGULAR STRENGTH

ASSORTED FRUIT

NATURALLY & ARTIFICIALLY FLAVORED

150 CHEWABLE TABLETS 71715XA

Principal Display Panel

TUMS®

CALCIUM RICH

ANTACID/CALCIUM SUPPLEMENT

REGULAR STRENGTH

PEPPERMINT

NATURALLY FLAVORED

150 CHEWABLE TABLETS 71716XA

TUMS  calcium carbonate   tablet

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0135-0071 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (CALCIUM CATION) CALCIUM CARBONATE 500 mg

Inactive Ingredients Ingredient Name Strength SUCROSE   STARCH, CORN   TALC   MINERAL OIL   ADIPIC ACID   SODIUM POLYMETAPHOSPHATE   FD&C RED NO. 40   FD&C YELLOW NO. 6   FD&C YELLOW NO. 5   FD&C BLUE NO. 1

Product Characteristics Color PINK (orange, yellow, green) Score no score Shape ROUND Size 16mm Flavor CHERRY (assorted fruit, orange, lemon, lime) Imprint Code TUMS Contains

Packaging # NDC Package Description Multilevel Packaging 1 0135-0071-01 180 TABLET In 1 BOTTLE None 2 0135-0071-03 3 PACKAGE In 1 CELLO PACK contains a PACKAGE 2 12 TABLET In 1 PACKAGE This package is contained within the CELLO PACK (0135-0071-03) 3 0135-0071-24 75 TABLET In 1 BOTTLE None 4 0135-0071-27 150 TABLET In 1 BOTTLE None 5 0135-0071-32 400 TABLET In 1 BOTTLE None 6 0135-0071-48 12 TABLET In 1 PACKAGE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	03/10/2010

TUMS  calcium carbonate   tablet

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 0135-0070 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (CALCIUM CATION) CALCIUM CARBONATE 500 mg

Inactive Ingredients Ingredient Name Strength SUCROSE   STARCH, CORN   TALC   MINERAL OIL   SODIUM POLYMETAPHOSPHATE

Product Characteristics Color WHITE Score no score Shape ROUND Size 16mm Flavor PEPPERMINT Imprint Code TUMS Contains

Packaging # NDC Package Description Multilevel Packaging 1 0135-0070-01 180 TABLET In 1 BOTTLE None 2 0135-0070-03 3 PACKAGE In 1 CELLO PACK contains a PACKAGE 2 12 TABLET In 1 PACKAGE This package is contained within the CELLO PACK (0135-0070-03) 3 0135-0070-24 75 TABLET In 1 BOTTLE None 4 0135-0070-27 150 TABLET In 1 BOTTLE None 5 0135-0070-48 12 TABLET In 1 PACKAGE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part331	03/10/2010

Labeler - GlaxoSmithKline Consumer Heathcare LP (091328625)

Revised: 03/2010GlaxoSmithKline Consumer Heathcare LP