REXALL ANTACID- calcium carbonate tablet, chewable
Dolgencorp, LLC

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.

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Dolgencorp, LLC Antacid Chews Drug Facts

Active ingredient (in each tablet)

Calcium carbonate USP 750mg

Purpose

Antacid

Uses

relieves

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

Warnings

Ask a doctor before use if you have

•: kidney stones
•: a calcium-restricted diet

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 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.

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 information

•: each tablet contains: calcium 320mg
•: store at 20-25°C (68-77°F)
•: does not meet USP for assay

Inactive ingredients

dextrose, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, flavors, glycerin, magnesium stearate, maltodextrin, mineral oil

Principal Display Panel

EXTRA STRENGTH

Antacid Chews

Calcium Carbonate 750 mg

Assorted Berries Flavors

750 mg

200 Chewable Tablets

REXALL ANTACID
calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:55910-708
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	750 mg

Ingredient Name	Strength
Inactive Ingredients
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MINERAL OIL (UNII: T5L8T28FGP)

Product Characteristics
Color	PINK (dark pink) , PINK (rose) , PURPLE (violet)	Score	no score
Shape	ROUND	Size	17mm
Flavor	BERRY (strawberry, raspberry, berry)	Imprint Code	L489
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:55910-708-82	200 in 1 BOTTLE; Type 0: Not a Combination Product	05/10/2011	02/01/2021

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	05/10/2011	02/01/2021

Labeler - Dolgencorp, LLC (068331990)

Revised: 1/2021

Document Id: 1ffb5511-f5bd-4067-b846-86e298386f86

Set id: 79dc5dd4-ae48-4add-9ab6-f509dac36408

Version: 5

Effective Time: 20210121

Dolgencorp, LLC