Active ingredient (per tablet)

Calcium Carbonate USP 1000mg

Purpose

Antacid

Uses

relieves

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

Warnings

Ask a doctor or pharmacist before use if you are

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

When using this product

•: do not take more than 7 tablets in 24 hours
•: if pregnant do not take more than 5 tablets in 24 hours
•: do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor

Keep out of reach of children.

Directions

•: adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor
•: do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Other information

•: each tablet contains: elemental calcium 400mg
•: store at room temperature. Keep the container tightly closed.

Inactive ingredients

adipic acid, D&C red #27 lake, D&C yellow #10 lake, dextrose, FD&C blue #1 lake, FD&C yellow #6 lake, flavors, magnesium stearate, maltodextrin, starch, sucralose.

Questions?

1-888-423-0139

Do Not Use

Do not use if printed seal under cap is torn or missing.

Principal Display Panel

+TopCare® healthTM

NDC# 36800-595-24

COMPARE TO ULTRA STRENGTH TUMS® ACTIVE INGREDIENT*

ULTRA STRENGTH

Antacid Tablets

CALCIUM CARBONATE 1000 mg

OUR PHARMACISTS RECOMMEND

FAST RELIEF OF:

•: Upset Stomach
•: Heartburn
•: Acid Indigestion

ASSORTED FRUIT FLAVORS

QUALITY GUARANTEED

GLUTEN FREE

72 CHEWABLE TABLETS

K PAREVE

DISTRIBUTED BY

TOPCO ASSOCIATES LLC

ELK GROVE VILLAGE, IL 60007

QUESTIONS? 1-888-423-0139

topcare@topco.com www.topcarebrand.com

Visit here for more information: http://topbrnds.com/48ZS22

*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Ultra Strength Tums®.

TOPCARE ANTACID CALCIUM ULTRA STRENGTH
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:36800-595
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	1000 mg

Ingredient Name	Strength
Inactive Ingredients
ADIPIC ACID (UNII: 76A0JE0FKJ)
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
D&C RED NO. 27 (UNII: 2LRS185U6K)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
STARCH, CORN (UNII: O8232NY3SJ)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	YELLOW, GREEN, RED, ORANGE	Score	no score
Shape	ROUND	Size	20mm
Flavor	FRUIT (lime, orange, cherry, lemon)	Imprint Code	L595
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:36800-595-24	72 in 1 BOTTLE; Type 0: Not a Combination Product	12/15/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M001	12/15/2018

Labeler - Topco Associates LLC (006935977)

Topco Associates LLC. Antacid Calcium Drug Facts