Label: ALUMINUM HYDROXIDE- aluminum hydroxide liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 16, 2024

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  • Active ingredient (in each 5 mL teaspoonful)

    Aluminum hydroxide 320 mg

  • Purpose

    Antacid



  • Uses

    relieves


    • heartburn
    • acid indigestion
    • sour stomach

  • Warnings

    taking a prescription drug. Antacids may interact with certain prescription drugs. you may get constipated symptoms last more than 2 weeks

    Ask a doctor or pharmacist before use if you are

    When using this product


    Stop use and ask a doctor if

    Keep out of reach of children.

  • Directions

    • shake well before using • do not take more than 12 teaspoonfuls in 24 hours • do not use the maximum dosage for more than 2 weeks • 2 teaspoonfuls 5-6 times daily after meals and at bedtime followed by a sip of water if needed




    dosage:
  • Other information

    • store at room temperature • protect from freezing  • keep tightly closed •


    TAMPER-EVIDENT: DO NOT USE IF FOIL SEAL UNDER CAP IS BROKEN OR MISSING.

  • Inactive ingredients

    benzyl alcohol, butylparaben, flavor, glycerin, hydroxyethylcellulose, propylparaben, purified water, saccharin sodium, simethicone emulsion, sorbitol solution

    Questions or comments?

    Call 9am - 5pm EST, Monday-Friday 1-800-645-2158

    DISTRIBUTED BY:

    ATLANTIC BIOLOGICALS CORP.

    MIAMI, FL 33179

  • ALUMINUM HYDROXIDE LIQUID

    image description

  • INGREDIENTS AND APPEARANCE
    ALUMINUM HYDROXIDE  
    aluminum hydroxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17856-0091(NDC:0536-0091)
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE320 mg  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINT (mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17856-0091-330 mL in 1 CUP; Type 0: Not a Combination Product04/16/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02/01/2005
    Labeler - ATLANTIC BIOLOGICALS CORP. (047437707)
    Registrant - ATLANTIC BIOLOGICALS CORP. (047437707)
    Establishment
    NameAddressID/FEIBusiness Operations
    UNIT DOSE SOLUTIONS360804194REPACK(17856-0091)
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