Mag-al Liquid

Manufacturer
A-S Medication Solutions
Effective date
2021-03-01
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:49:52

Label at a glance#

ProductMag-al Liquid
Active ingredientALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE
Label structure12 sections

Indications and uses

for the relief of: acid indigestion heartburn sour stomach upset stomach due to these symptoms

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 weeks adults and children 12 years and older take 2 to 4 teaspoonfuls four times a day or as directed by a physician children under 12 years consult a physician

Storage and handling

each 5 mL contains: magnesium 83 mg, sodium 1.34 mg does not meet USP requirements for preservative effectiveness store at controlled room temperature 20° - 25°C (68° - 77°F) protect from freezing White colored, peppermint flavored liquid supplied in the following oral dosage form: NDC 0121-1760-30: 30 mL unit dose cup. Case contains 100 unit dose cups of 30 mL packaged in 10 trays of 10 unit dose cups each. *Maal...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredients (in each 5 mL = 1 teaspoonful)Purpose
Aluminum hydroxide (equiv. to dried gel, USP) 200 mgAntacid
Magnesium hydroxide 200 mgAntacid

Uses

INDICATIONS & USAGE SECTION

for the relief of:

  • acid indigestion
  • heartburn
  • sour stomach
  • upset stomach due to these symptoms

Warnings

WARNINGS SECTION

Do not take 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 physician.

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 more than 2 weeks.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

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 weeks
adults and children 12 years and oldertake 2 to 4 teaspoonfuls four times a day or as directed by a physician
children under 12 yearsconsult a physician

Other information

STORAGE AND HANDLING SECTION

  • each 5 mL contains: magnesium 83 mg, sodium 1.34 mg
  • does not meet USP requirements for preservative effectiveness
  • store at controlled room temperature 20° - 25°C (68° - 77°F)
  • protect from freezing
  • White colored, peppermint flavored liquid supplied in the following oral dosage form:
NDC 0121-1760-30:30 mL unit dose cup. Case contains 100 unit dose cups of 30 mL packaged in 10 trays of 10 unit dose cups each.

*Maalox is a registered trademark of Novartis Consumer Health, Inc.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Antifoam af emulsion, butylparaben, hydroxypropyl methylcellulose, flavoring, propylene glycol, propylparaben, purified water, sodium saccharin, and sorbitol solution.

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-845-8210

SPL UNCLASSIFIED SECTION

MANUFACTURED BY

Pharmaceutical
Associates, Inc.

Greenville, SC 29605

R05/19

HOW SUPPLIED

HOW SUPPLIED SECTION

Product: 50090-2802

NDC: 50090-2802-0 10 mL in a TRAY / 10 in a CASE

Storage

STORAGE AND HANDLING SECTION

store at controlled room temperature 20° - 25°C (68° - 77°F) protect from freezing

Aluminum Hydroxide and Magnesium Hydroxide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label Image
Label Image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-2802-02023-02-07C16284748780-1f386c64a-38a2-0266-e053-dadaa90a7c1aMag-al Liquid
50090-2802-02023-01-30C16284748780-1f386c64a-38a2-0266-e053-dadaa90a7c1aMag-al Liquid

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2802-0ML - Milliliter50090-2802c6d24eac-1916-4f55-80cf-842d41ad46ac12021-09-07
0121-1760-30ML - Milliliter0121-1760a959079c-4307-4f87-abd6-eb39a2359c8b12014-10-03

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50090-280250090-2802-0
0121-1760

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mag-AL LiquidALUMINUM HYDROXIDE AND MAGNESIUM HYDROXIDEPAI Holdings, LLCb1f2d137-f5f7-4800-a1df-ef5d25544bc92024-10-08WarningsExact identifier
ndc (product): 0121-1760
ff2e16af-f705-4500-9aed-3a88c345ec205fe0fe0b-db08-40a4-9bbf-90b9193743202023-02-06WarningsExact identifier
spl set id: 5fe0fe0b-db08-40a4-9bbf-90b919374320

Reported adverse events (FAERS/openFDA)#

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