HEB ® Extra Strength Chewable Tablets Cherry Flavor

Manufacturer
HEB
Effective date
2026-09-18
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
daily-update
Hydrated at
2026-09-22 03:02:28

Label at a glance#

ProductHEB Extra Strength Cherry 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 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
  • on a sodium-restricted diet
  • do not use for peptic ulcers.

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 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, natural and artificial flavor, sodium bicarbonate, starch (corn), sucrose.

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HEB®

NDC 37808-510-10

Antacid Tablets

Compare To Gaviscon®Extra Strength active ingredients*

EXTRA STRENGTH

Aluminum Hydroxide, 160 mg

Magnesium Carbonate, 105 mg

  • Long Lasting Antacid Barrier
  • Fast-Acting Heartburn Relief

Cherry Flavor

Naturally and Artificially Flavored

100 CHEWABLE TABLETS

MADE WITH PRIDE & CARE FOR H-E-B

SAN ANTONIO, TX 78204

100% GUARANTEE Promise

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.

HEB Antacid Tablets Cherry Flavor 100 counts
HEB Antacid Tablets Cherry Flavor 100 counts

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130041220616060GTIN-13: 0041220616060
EAN-13: 0041220616060
GTIN-12: 041220616060
UPC-A: 041220616060
GTIN storage (14 digits): 00041220616060
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

FDA-Initiated Inactive NDC Indexing#

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
37808-51037808-510-10

Ingredients#

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

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

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52025-10-03full-release2026-06-01 01:15:47

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
403e8533-17f3-670d-e063-6394a90a5b2a6e10ad65-5baf-4763-befe-ed046bf914b52025-10-03WarningsExact identifier
spl set id: 6e10ad65-5baf-4763-befe-ed046bf914b5

Reported adverse events (FAERS/openFDA)#

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