Label: SODIUM BICARBONATE 10GR (650MG)- sodium bicarbonate tablet

  • NDC Code(s): 45861-081-10
  • Packager: Pharmaceutica North America, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 14, 2025

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  • Active ingredient (in each tablet)

    Sodium bicarbonate 10 gr (650 mg)

  • Purpose

    Antacid

  • Uses

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

  • Warnings

    Ask a doctor before use if you havea sodium restricted diet.
    Ask a doctor or pharmacist before use if you aretaking a prescription drug.
    Antacids may interact with certain prescription drugs.
    Stop use and ask a doctor ifsymptoms last more than 2 weeks
    If pregnant or breast-feeding, ask a health professional before use.
    Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    • do not use the maximum dosage for more than 2 weeks
    • tablets may be swallowed whole or dissolved in water prior to use
    • adults 60 years of age and over: 1-2 tablets every 4 hours, not more than 12 tablets in 24 hours
    • adults under 60 years of age: 1-4 tablets every 4 hours, not more than 24 tablets in 24 hours

  • Other information

    • each tablet contains: sodium 178 mg
    • store in a dry place at 15° – 30°C (59° – 86°F).

  • Inactive Ingredients

    croscarmellose sodium, microcrystalline cellulose, silica, stearic acid, talc.

  • Questions or comments? (888)788-6472

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    SODIUM BICARBONATE 10GR (650MG) 
    sodium bicarbonate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45861-081
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE650 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    Colorwhite (Off White) Scoreno score
    ShapeROUNDSize11mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:45861-081-101000 in 1 BOTTLE; Type 0: Not a Combination Product02/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00102/01/2025
    Labeler - Pharmaceutica North America, Inc. (962739699)
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