FDA.reportPublic FDA data

Quality Choice Antacid Tablets Extra Strength Original Flavor

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC.
Effective date
2025-12-03
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:19:24

Label at a glance#

ProductExtra Strength Antacid Original Flavor
Active ingredientALUMINUM HYDROXIDE, MAGNESIUM CARBONATE
Label structure8 sections

Indications and uses

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

Dosage and administration

chew 2 to 4 tablets four times a day or as directed by a doctor take after meals and at bedtime or as needed for best results follow by a half glass of water or other liquid DO NOT SWALLOW WHOLE

Label contents#

Full prescribing information#

Active ingredients (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Aluminum hydroxide 160 mg

Magnesium carbonate 105 mg

Purpose

OTC - PURPOSE SECTION

Antacid

Antacid

Uses

INDICATIONS & USAGE SECTION

relieves

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

Warnings

WARNINGS SECTION

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • taking a prescription drug. Antacids may interact with certain prescription drugs
  • on a sodium-restricted diet

When using this product

OTC - WHEN USING SECTION

  • do not take more than 16 tablets in 24 hours
  • do not use the maximum dosage for more than 2 weeks

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center immediately.

1-800-222-1222

Directions

DOSAGE & ADMINISTRATION SECTION

  • chew 2 to 4 tablets four times a day or as directed by a doctor
  • take after meals and at bedtime or as needed
  • for best results follow by a half glass of water or other liquid
  • DO NOT SWALLOW WHOLE

Other information

SPL UNCLASSIFIED SECTION

  • each tablet contains:sodium 19 mg, magnesium 31 mg.
  • Store at up to 25°C (77°F) in a dry place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

alginic acid, calcium stearate, compressible sugar, flavor, sodium bicarbonate, starch (corn), sucrose.

Questions or comments

OTC - QUESTIONS SECTION

1-866-467-2748

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

QUALITY CHOICE®

NDC 63868-996-01

Compare To Gaviscon® active ingredients*

Extra Strength

Antacid Tablets

Foaming

Long Lasting Antacid Barrier

Fast Acting Heartburn Relief

Original Flavor

100% QC SATISFACTION GUARANTEED

  • DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING.
  • Distributed by C.D.M.A., Inc.©
  • 43157 W. Nine Mile
  • Novi, MI 48376-0995
  • www.qualitychoice.com
  • Questions: 248-449-9300

*This product is not manufactured or distributed by GlaxoSmithKline, the distributor of Gaviscon ®Extra Strength.

Extra Strength Antacid Tablets Original Flavor 100 Chewable Tablets
Extra Strength Antacid Tablets Original Flavor 100 Chewable Tablets

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308072aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable TabletPSN6
308072aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable TabletSCD6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130635515950795GTIN-13: 0635515950795
EAN-13: 0635515950795
GTIN-12: 635515950795
UPC-A: 635515950795
GTIN storage (14 digits): 00635515950795		35d01fe6-542e-41fe-a81b-49e1077a7e8e-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-996-01Extra Strength AntacidOriginal Flavor100 in 1 BOTTLE, PLASTICTABLET, CHEWABLE1006

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-996-01EA - Each63868-9962daeb452-3964-4a5c-9c71-9df32b8c466e12019-05-02

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63868-99663868-996-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALGINIC ACID8C3Z4148WZIACT
CALCIUM STEARATE776XM7047LIACT
CORN SYRUP9G5L16BK6NIACT
SODIUM BICARBONATE8MDF5V39QOIACT
STARCH, CORNO8232NY3SJIACT
SUCROSEC151H8M554IACT
ALUMINUM HYDROXIDE5QB0T2IUN0ACTIB
MAGNESIUM CARBONATE0E53J927NAACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Extra Strength Antacid Original FlavorALUMINUM HYDROXIDE AND MAGNESIUM CARBONATECHAIN DRUG MARKETING ASSOCIATION INC.8064b01a-e049-4d49-a5b6-e72dbeb5daac2025-12-03WarningsExact identifier
ndc (package): 63868-996-01
ndc (product): 63868-996
ndc11 (package): 63868099601
spl id: 450950a9-ab67-e524-e063-6394a90a7160
spl set id: 8064b01a-e049-4d49-a5b6-e72dbeb5daac

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.