Label: INON ACE- magnesium aluminosilicate, magnesium hydroxide solution

  • NDC Code(s): 49873-403-01
  • Packager: Sato Pharmaceutical Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 6, 2023

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  • ACTIVE INGREDIENT

    Active ingredients (in each bottle)
    Magnesium Aluminosilicate 900 mg
    Magnesium Hydroxide 250 mg

  • PURPOSE

    Purpose
    Magnesium Aluminosilicate     Antacid
    Magnesium Hydroxide     Antacid

  • INDICATIONS & USAGE

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

  • WARNINGS

    Warnings

    Do not use this product if you are taking a prescription antibiotic drug containing any
    form of tetracycline.

    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 2 bottles (adults and children 12 years and over) in a 24-hour 
        period or use the maximum dosage of this product for more than 2 weeks, except under
        the advice and supervision of a physician.
    ■ may have a laxative effect.

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

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Directions
    ■ adults and children 12 years and over: Take 1 bottle (30mL) at a time 2 times daily,    
        between meals, or as directed by a doctor.
    ■ children under 12 years: Ask a doctor.
    ■ shake well before use.

  • OTHER SAFETY INFORMATION

    Other information
    ■ each bottle contains: sodium 15 mg, magnesium 165 mg

  • INACTIVE INGREDIENT

    Inactive ingredients  alcohol, butylparaben, citric acid, flavors (cinnamon oil, fluid
    extract of ginger root, spearmint oil), hydroxypropylstarch, PEG-60 hydrogenated castor
    oil, propylparaben, sodium benzoate, sodium citrate, sorbitol, water.

  • PRINCIPAL DISPLAY PANEL

    carton

  • INGREDIENTS AND APPEARANCE
    INON ACE 
    magnesium aluminosilicate, magnesium hydroxide solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49873-403
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILODRATE (UNII: 9T3UU8T0QK) (SILODRATE - UNII:9T3UU8T0QK) SILODRATE900 mg  in 30 mL
    MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE250 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLPARABEN (UNII: 3QPI1U3FV8)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT) (UNII: 9M44R3409A)  
    POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorCINNAMON (CINNAMON OIL) , MINT (MENTHA OIL) , GINGER (GINGER, LIQUID EXTRACT) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49873-403-012 in 1 CARTON05/20/2000
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00105/20/2000
    Labeler - Sato Pharmaceutical Co., Ltd. (690575642)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sato Pharmaceutical Co., Ltd.715699133manufacture(49873-403) , label(49873-403) , pack(49873-403)
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