Antacid Mint

Manufacturer
Walgreens
Effective date
2023-01-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:40:13

Label at a glance#

ProductAntacid Mint
Active ingredientALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONE
Label structure14 sections

Indications and uses

For the relief of acid indigestion heartburn sour stomach upset stomach associated with these symptoms pressure and bloating commonly referred to as gas

Dosage and administration

shake well before using do not take more than 16 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 week adults and children 12 years of age and older: take 2 to 4 teaspoonfuls four times a day or as directed by a physican children under 12 years of age: do not use

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Aluminum hydroxide (equiv. to dried gel, USP) 200 mg
Magnesium hydroxide 200 mg
Simethicone 20 mg

Purpose

OTC - PURPOSE SECTION

Antacid

Antacid

Antigas

Uses

INDICATIONS & USAGE SECTION

  • For the relief of
    • acid indigestion
    • heartburn
    • sour stomach
    • upset stomach associated with these symptoms
    • pressure and bloating commonly referred to as gas

Warnings

WARNINGS SECTION

Do not take

OTC - DO NOT USE SECTION

more than 16 teaspoonfuls in a 24-hour period or use the maximum dosage for more than 2 weeks except under the advice and supervision of a physican

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

• kidney disease • a magnesium restricted diet

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

presently taking a prescription drug. Antacids may interact with certain prescription drugs.

Stop use and ask a doctor if

OTC - STOP USE SECTION

symptoms last for more than 2 weeks

If pregnant or breast-feeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep  out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Controls Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • shake well before using
  • do not take more than 16 teaspoonfuls in 24 hours or use the maximum dosage for more than 2 week
  • adults and children 12 years of age and older: take 2 to 4 teaspoonfuls four times a day or as directed by a physican
  • children under 12 years of age: do not use

Other Information

SPL UNCLASSIFIED SECTION

  • each teaspoon (5 mL) contains: magnesium 80 mg, potassium 5 mg, and sodium 2 mg
  • store between 20-25ºC (68-77ºF). Avoid freezing

Inactive Ingredients

INACTIVE INGREDIENT SECTION

benzyl alcohol, carboxymethylcellose sodium, flavors, glycerin, microcrystalline cellulose, potassium citrate, propylene glycol, purified water, sorbitol, saccharin sodium xanthan gum

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to Maalox® Advanced Regular Strength Active ingredient††

Antacid +

Anti-Gas Liquid

ALUMINUM HYDROXIDE 200 mg / ANTACID

MAGNESIUM HYDROXIDE 200 mg / ANTACID

SIMETHICONE 20 mg /ANTI-GAS

REGULAR STRENGTH

  • Fast relief of heartburn, pressure, bloating & acid indigestion

FL OZ (mL)

MINT FLAVOR

††This product is not manufactured or distributed by Novartis Consumer Health, Inc., distributor of Maalox® Advanced Regular Strength.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.

DISTRIBUTED BY: WALGREENS CO.,

200 WILMOT RD., DEERFIELD, IL 60015

walgreens.com


Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-0432-12ML - Milliliter0363-0432e9a3bef9-fbb5-4eff-9186-cfdef900d01212019-08-06
0363-0432-26ML - Milliliter0363-0432f62aab9e-d1ef-4abf-a932-b8223c8b51a212019-10-07

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-04320363-0432-26, 0363-0432-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
1ffb530b-0302-469b-b058-8acdbfe1d83cfbe71cba-a868-4d9d-9616-349bfcaa4f642023-01-18WarningsExact identifier
spl id: 1ffb530b-0302-469b-b058-8acdbfe1d83c
spl set id: fbe71cba-a868-4d9d-9616-349bfcaa4f64

Reported adverse events (FAERS/openFDA)#

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