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NDC 69842-0396-54 Extra Strength Antacid 750 mg/1 Details

Extra Strength Antacid 750 mg/1

Extra Strength Antacid is a ORAL TABLET, CHEWABLE in the HUMAN OTC DRUG category. It is labeled and distributed by CVS PHARMACY, INC.. The primary component is CALCIUM CARBONATE.

MedlinePlus Drug Summary

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Related Packages: 69842-0396-54
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Calcium Carbonate

Product Information

NDC	69842-0396
Product ID	69842-396_60ea7f8f-808e-403f-a349-474a3247b2c5
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Extra Strength Antacid
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium Carbonate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, CHEWABLE
Route	ORAL
Active Ingredient Strength	750
Active Ingredient Units	mg/1
Substance Name	CALCIUM CARBONATE
Labeler Name	CVS PHARMACY, INC.
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part331
Listing Certified Through	2024-12-31

Package

Package Images

NDC 69842-0396-54 (69842039654)

Pricing Information	N/A
NDC Package Code	69842-396-54
Billing NDC	69842039654
Package	15 POUCH in 1 CARTON (69842-396-54) / 2 TABLET, CHEWABLE in 1 POUCH
Marketing Start Date	2017-12-13
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 80e10be2-879b-47ba-b34d-a3c25e838e05 Details

Active ingredient (per tablet)

Calcium Carbonate USP 750 mg

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 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

SPL UNCLASSIFIED SECTION

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 300 mg
store at room temperature 15° - 30°C (59° - 86°F)

Inactive ingredients

dextrose, flavor (peppermint), maltodextrin, magnesium stearate

Questions or comments?

Call toll free: 1-855-215-8180

PRINCIPAL DISPLAY PANEL

Extra Strength Antacid Tablets

30 Tablets 15 Pouches (2 Tablets per Pouch)

NDC 69842-396-54

INGREDIENTS AND APPEARANCE

EXTRA STRENGTH ANTACID

calcium carbonate tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:69842-396
Route of Administration	ORAL

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

Ingredient Name	Strength
Inactive Ingredients
DEXTROSE (UNII: IY9XDZ35W2)
PEPPERMINT (UNII: V95R5KMY2B)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	16mm
Flavor	PEPPERMINT	Imprint Code	AP;052
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:69842-396-54	15 in 1 CARTON	12/13/2017
1		2 in 1 POUCH; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part331	12/13/2017

Labeler - CVS PHARMACY, INC. (062312574)

Name	Address	ID/FEI	Business Operations
Establishment
Advance Pharmaceutical Inc.		078301063	manufacture(69842-396)

Revised: 12/2017

Document Id: 60ea7f8f-808e-403f-a349-474a3247b2c5

Set id: 80e10be2-879b-47ba-b34d-a3c25e838e05

Version: 1

Effective Time: 20171213