Label: ANTACID AND ANTIGAS- calcium carbonate, magnesium hydroxide, simethicone liquid

  • NDC Code(s): 57896-662-12
  • Packager: Geri-Care Pharmaceuticals, Corp
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 30, 2025

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  • Active ingredients (in each 10 mL dose)

    Calcium carbonate 800 mg
    Magnesium hydroxide 270 mg
    Simethicone 80 mg

  • Purposes

    Antacid

    Antigas

  • Uses

    relieves

    • heartburn
    • sour stomach
    • acid indigestion
    • the symptoms referred to as gas
    • upset stomach assiciated with these symptoms

  • 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.

    Stop use and ask a doctor if symptoms last for more than 2 weeks

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

  • Directions

    • shake well before use
    • adults and children 12 years of age and older: take 10 mL to 20 mL (1 to 2 doses) between meals as needed, at bedtime,

    or as directed by a doctor

    • do not take more than 60 mL (6 doses) in any 24-hour period or use the maximum dosage for more than 2 weeks
    • children under 12 years of age: ask a doctor
    • mL = milliliter
  • Other information

    • each 10 mL dose contains: calcium 320 mg, magnesium 115 mg
    • do not freeze
    • store at room temperature tightly closed
  • Inactive ingredients

    benzyl alcohol, flavor, purified water, simethicone emulsion, sorbic acid, sorbitol solution, sucralose, xanthan gum

  • Questions or comments?

    1-800-540-3765

  • package Label

    1

  • INGREDIENTS AND APPEARANCE
    ANTACID AND ANTIGAS 
    calcium carbonate, magnesium hydroxide, simethicone liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57896-662
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE800 mg  in 10 mL
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE80 mg  in 10 mL
    MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE270 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    SORBIC ACID (UNII: X045WJ989B)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    WATER (UNII: 059QF0KO0R)  
    SORBITOL SOLUTION (UNII: 8KW3E207O2)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorHONEY (honey camomile) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57896-662-12355 mL in 1 BOTTLE; Type 0: Not a Combination Product12/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00112/01/2025
    Labeler - Geri-Care Pharmaceuticals, Corp (611196254)
    Registrant - GCP Laboratories (965480861)
    Establishment
    NameAddressID/FEIBusiness Operations
    GCP Laboratories965480861manufacture(57896-662) , pack(57896-662)
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