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ACID GONE ANTACID (Major Pharmaceuticals)

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LIQUID 355 mL in 1 BOTTLE (0904-7727-14) Label Information

Complete ACID GONE ANTACID Information

  • Active ingredient (in each 15mL tablespoonful)

    Aluminum hydroxide 95mg

    Magnesium carbonate 358mg


  • Purpose

    Antacid


  • Uses

    relieves

    • heartburn
    • acid indigestion
    • sour stomach
    • upset stomach associated with these symptoms

  • Warnings

    Ask a doctor before use if you have

    • kidney disease
    • a magnesium-restricted diet
    • 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.
    When using this product

    • do not take more than 8 tablespoonfuls in 24 hours
    • do not use the maximum dosage for more than 2 weeks
    • laxative effect may occur

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


  • Keep out of reach of children.

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


  • Directions

    • shake well before use
    • adults and children 12 years and older: take 1 to 2 tablespoonfuls four times a day or as directed by a doctor
    • children under 12 years: ask a doctor
    • take after meals and at bedtime
    • dispense product only by spoon or other measuring device

  • Other information

    • each 15 mL tablespoonful contains: magnesium 105mg, sodium 39mg
    • store at up to 25°C (77°F)
    • avoid freezing
    • keep tightly closed
    • TAMPER-EVIDENT: Do not use this product if inner foil seal over the mouth of the bottle is broken or missing.

  • Inactive ingredients (Regular Strength)

    benzyl alcohol, D&C yellow #10, edetate disodium, FD&C blue #1, flavor, glycerin, purified water, saccharin sodium, sodium alginate, sorbitol solution, xanthan gum


  • Questions or comments?

    1-800-540-3765


  • Principal Display Panel

    major

    NDC 0904-7727-14

    Acid Gone Antacid

    Alumina and Magnesium Carbonate
    Oral Suspension USP

    Relieves Heartburn
    & Acid Indigestion

    Compare to the active ingredients in Gaviscon® *

    12 FL OZ (355 mL)

    MAJ


  • INGREDIENTS AND APPEARANCE
    ACID GONE ANTACID 
    aluminum hydroxide and magnesium carbonate liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0904-7727
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 95 mg  in 15 mL
    MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE 358 mg  in 15 mL
    Inactive Ingredients
    Ingredient Name Strength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM ALGINATE (UNII: C269C4G2ZQ)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    Color green Score     
    Shape Size
    Flavor SPEARMINT (cool mint) Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0904-7727-14 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2017
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part331 12/30/2004
    Labeler - Major Pharmaceuticals (191427277)
    Registrant - GCP Laboratories (965480861)
    Establishment
    Name Address ID/FEI Business Operations
    GCP Laboratories 965480861 manufacture(0904-7727)