ULTRA STRENGTH ANTACID- calcium carbonate tablet, chewable

Ultra strength Antacid by

Drug Labeling and Warnings

Ultra strength Antacid 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 1000 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 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.

DOSAGE & ADMINISTRATION

Directions

• adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor. Chew or crush tablets completely before swallowing.
• 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 400 mg, magnesium 12mg
• store at room temperature. Keep the container tightly closed

INACTIVE INGREDIENT

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

QUESTIONS

Questions or comments? Call 1-877-290-4008

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ULTRA STRENGTH ANTACID 
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51316-905
Route of Administration	ORAL

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

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

Product Characteristics
Color	orange (yellow, green, pink)	Score	no score
Shape	ROUND	Size	19mm
Flavor	FRUIT (Assorted Fruit(Orange, Lemon, Lime Marvel, Strawberry))	Imprint Code	T472
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51316-905-66	160 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2025
2	NDC: 51316-905-75	72 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(51316-905)