EXTRA STRENGTH ANTACID CALCIUM CARBONATE, 750MG- calcium carbonate chewable tablets tablet, chewable

Extra Strength Antacid Calcium Carbonate, 750mg by

Drug Labeling and Warnings

Extra Strength Antacid Calcium Carbonate, 750mg by is a Otc medication manufactured, distributed, or labeled by CVS HEALTH CORP, TIME CAP LABORATORIES, INC., MARKSANS PHARMA LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active ingredient (per tablet)

Calcium Carbonate USP 750 mg

PURPOSE

Purpose

Antacid

INDICATIONS & USAGE

Uses relieves

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

WARNINGS

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

When using this product

• do not take more than 10 tablets in 24 hours
• if pregnant do not take more than 6 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

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions

• adults and children 12 years of age and over: chew 2-4 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 SAFETY INFORMATION

Other information

• each tablet contains: elemental calcium 300 mg, magnesium 8 mg
• store at room temperature. Keep the container tightly closed.

INACTIVE INGREDIENT

Inactive ingredients adipic acid, corn starch, D&C red 27 lake, D&C yellow 10 Al lake, dextrose anhydrous, FD&C blue no. 1 Al lake, FD&C yellow #6 lake, flavors, magnesium stearate, maltodextrin, sucralose

QUESTIONS

Questions or comments?

Call 1-877-290-4008

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EXTRA STRENGTH ANTACID CALCIUM CARBONATE, 750MG 
calcium carbonate chewable tablets tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-636
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB)	CALCIUM CARBONATE	750 mg

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
FD&C YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q)
D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)
D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)
FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)
ADIPIC ACID (UNII: 76A0JE0FKJ)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	orange (light yellow, light green, mottled pink)	Score	no score
Shape	ROUND	Size	16mm
Flavor	FRUIT (Assorted Fruit(Orange, Lemon, Lime marvel, strawberry))	Imprint Code	T;471
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-636-69	96 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2025
2	NDC: 51316-636-25	250 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	04/01/2025

Labeler - CVS HEALTH CORP (062312574)

Registrant - TIME CAP LABORATORIES, INC. (037052099)

Establishment
Name	Address	ID/FEI	Business Operations
MARKSANS PHARMA LIMITED		677604129	manufacture(51316-636)