FDA.reportPublic FDA data

Extra Strength Antacid Chewable Tablets Original Flavor

Manufacturer
TARGET CORPORATION
Effective date
2025-11-04
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:41:53

Label at a glance#

ProductExtra Strength Antacid
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 completely 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 TABLETS 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
  • If you are 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 at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

  • chew 2 to 4 tablets completely 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 TABLETS WHOLE

Other information

SPL UNCLASSIFIED SECTION

  • each tablet contains:magnesium 31 mg, sodium 19 mg
  • Store at room temperature.

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

NDC 11673-814-00

Compare to the active ingredients in Gaviscon®Extra Strength Antacid*

Extra Strength

Antacid Tablets

Aluminum Hydroxide

Magnesium Carbonate

  • Fast-Acting Heartburn Relief
  • Helps Keep Acid Down for Hours

Original Flavor

100 Chewable Tablets

WARNING: Consuming this product can expose you to chemicals including lead, which is known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov

Distributed by Target Corporation, Minneapolis, MN 55403

Made in U.S.A

TM & ©2020 Target Brands, Inc.

DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING

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

Extra Strength Antacid Tablets 100 Chewable Tablets
Extra Strength Antacid Tablets 100 Chewable Tablets

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
308072aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable TabletPSN8
308072aluminum hydroxide 160 MG / magnesium carbonate 105 MG Chewable TabletSCD8

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130368163105100GTIN-13: 0368163105100
EAN-13: 0368163105100
GTIN-12: 368163105100
UPC-A: 368163105100
GTIN storage (14 digits): 00368163105100		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
11673-814-00Extra StrengthAntacid100 in 1 BOTTLE, PLASTICTABLET, CHEWABLE1008

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
11673-81411673-814-00

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
72024-11-07full-release2026-06-01 00:35:33

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 AntacidALUMINUM HYDROXIDE AND MAGNESIUM CARBONATETARGET CORPORATION3d987f0b-4d7e-489e-ab19-efe1ee11009a2025-11-04WarningsExact identifier
ndc (package): 11673-814-00
ndc (product): 11673-814
ndc11 (package): 11673081400
spl id: 42c242a8-b691-c001-e063-6394a90ae4a4
spl set id: 3d987f0b-4d7e-489e-ab19-efe1ee11009a

Reported adverse events (FAERS/openFDA)#

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