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
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated December 31, 2020

If you are a consumer or patient please visit this version.

  • 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 finalpart33105/31/1989
    Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sato Pharmaceutical Co., Ltd.715699133manufacture(49873-045) , label(49873-045) , pack(49873-045)