Label: INON- aluminum hydroxide, magnesium carbonate, sodium bicarbonate granule

  • NDC Code(s): 49873-045-01
  • Packager: Sato Pharmaceutical Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 4, 2023

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  • ACTIVE INGREDIENT

    Active ingredients [in each packet (1.92g)]
    Aluminum hydroxide 400 mg
    Magnesium carbonate 400 mg
    Sodium bicarbonate 700 mg

  • PURPOSE

    Purpose
    Aluminum hydroxide     Antacid
    Magnesium carbonate     Antacid
    Sodium bicarbonate     Antacid

  • INDICATIONS & USAGE

    Uses relieves these symptoms
    ■ heartburn    ■ sour stomach    ■ acid indigestion

  • WARNINGS

    Warnings

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

    When using this product

    ■ Do not take more than 3 packets in 24-hours period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor

    ■ May have laxative effect


    Ask a doctor before use if you have

    ■ a sodium-restricted diet

    Ask a doctor or pharmacist before use if you are

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

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions
    ■ Adults and children 12 years of age and over: Take 1 packet at a time 3 times daily between meals or after meals, or as directed by a doctor
    ■ Children under 12 years: Ask a doctor

  • OTHER SAFETY INFORMATION

    Other information ■ Each packet contains: sodium 175 mg, magnesium 95 mg

  • INACTIVE INGREDIENT

    Inactive ingredients  colloidal silicon dioxide, flavor, partially hydrolyzed polyvinyl alcohol, sugar, starch

  • PRINCIPAL DISPLAY PANEL

    inongrancart.jpg carton


  • INGREDIENTS AND APPEARANCE
    INON 
    aluminum hydroxide, magnesium carbonate, sodium bicarbonate granule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-045
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE400 mg  in 1.92 g
    MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE400 mg  in 1.92 g
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE700 mg  in 1.92 g
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    POLYVINYL ALCOHOL (UNII: 532B59J990)  
    SUCROSE (UNII: C151H8M554)  
    STARCH, POTATO (UNII: 8I089SAH3T)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorPEPPERMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49873-045-0112 in 1 CARTON05/31/1989
    11.92 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00105/31/1989
    Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sato Pharmaceutical Co., Ltd.715699133manufacture(49873-045) , label(49873-045) , pack(49873-045)
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