Label: MAG-AL PLUS- aluminum hydroxide, magnesium hydroxide, and simethicone suspension

  • NDC Code(s): 0121-1761-30
  • Packager: PAI Holdings, LLC dba PAI Pharma
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated August 19, 2026

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredients (in each 30 mL dose)

    Aluminum hydroxide (equiv. to dried gel, USP)    1200 mg
    Magnesium hydroxide    1200 mg
    Simethicone       120 mg

  • Purposes

    Antacid

    Antigas

  • USES

    Uses relieves

    • acid indigestion
    • heartburn
    • sour stomach
    • upset stomach due to these symptoms
    • gas associated with heartburn, sour stomach or acid indigestion
  • Warnings

    Ask a doctor before use if you have

    • kidney disease
    • a magnesium-restricted diet

    Ask a doctor or pharmacist before use if you are

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

    When using this product

    • do not take more than 60 mL (2 doses) in a 24-hour period
    • do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor
    • may cause a laxative effect

    If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children. In case of overdose, get medical help or contact a poison control center right away.

  • Directions

    • shake well before using
    • mL = milliliters
    • adults and children 12 years of age and older: 30 mL (1 dose) up to 2 times a day or as directed by a doctor
    • children under 12 years of age: ask a doctor
  • Other information

    • each 30 mL contains: magnesium 535 mg, sodium 2 mg
    • store at 20° to 25°C (68° to 77°F)
    • protect from freezing
    • tamper-evident: do not use if seal on cup is missing or torn
  • INACTIVE INGREGIENTS

    Inactive ingredients butylparaben, hydroxypropyl methylcellulose, flavoring, propylene glycol, propylparaben, purified water, saccharin sodium, sorbitol solution

  • QUESTIONS OR COMMENTS?

    Questions or comments? Call 1-800-845-8210

  • SPL UNCLASSIFIED SECTION

    White colored, peppermint flavored liquid supplied in the following oral dosage form:
    NDC 0121-1761-30: 30 mL unit dose cup, in a tray of ten cups.

    Distributed by:
    PAI Pharma
    Greenville, SC 29605
    www.paipharma.com

    R05/26

  • PRINCIPAL DISPLAY PANEL - 30 mL Unit-Dose Cup

    Delivers 30 mL

    NDC 0121-1761-30

    MAG-AL PLUS™

    Aluminum Hydroxide  1200 mg / Antacid
    Magnesium Hydroxide  1200 mg / Antacid
    Simethicone  120 mg / Antigas

    SHAKE WELL

    Package Not Child-Resistant

    Dist. by: PAI Pharma
    Greenville, SC 29605
    SEE DRUG FACTS INSERT

     

    F0761300526

    30 mL lidding for MAG AL Plus
  • INGREDIENTS AND APPEARANCE
    MAG-AL PLUS 
    aluminum hydroxide, magnesium hydroxide, and simethicone suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0121-1761
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE1200 mg  in 30 mL
    MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838, HYDROXIDE ION - UNII:9159UV381P) MAGNESIUM HYDROXIDE1200 mg  in 30 mL
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE120 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    HYPROMELLOSE 2910 (4000 MPA.S) (UNII: RN3152OP35)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SORBITOL (UNII: 506T60A25R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorPEPPERMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0121-1761-3010 in 1 CASE01/14/2004
    110 in 1 TRAY
    130 mL in 1 CUP, UNIT-DOSE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00101/14/2004
    Labeler - PAI Holdings, LLC dba PAI Pharma (044940096)
    Establishment
    NameAddressID/FEIBusiness Operations
    PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma097630693manufacture(0121-1761)
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