Label: RAPIDOL SODIUM BICARBONATE- sodium bicarbonate powder

  • 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 March 6, 2023

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  • Drug Facts

  • Active Ingredient & Purposes

    Active ingredient (in each ½ teaspoon) Purpose
    Sodium bicarbonate 2,616 mg.........................................................................................................Antacid

  • Uses For the relief of an upset stomach associated with these symptoms

    • heatburn
    • sour stomach
    • acid indigestion
  • Warnings

    Stomach Waring: To avoid serious injury, do not take powder until it is completely dissolved. It is very important not to take this product when overly full from food or drink. Consult a doctor if severe stomach pain occurs after taking this product.

    Do not use

    • the maximum daily dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor
    • this product except under advice and supervision of a physician if you are allergic to milk or milk products

    When using this product

    • may cause constipation
    • may have laxative effect

    Ask a doctor or pharmacist before use if you are

    • presently taking a prescription drug. Antacids may interact with certain prescription drugs.

    Ask a doctor before use if you have

    • a sodium-restricted diet

    If pregnant or breast-feeding,

    ask a health professional before use.

    KEEP OUT OF REACH OF CHILDREN.

    In case of an accidental overdose, seek professional assistance or contact a Poison Control center right away.

  • Directions

    • do not take more than your “ maximum daily dosage for your age group” in a 24-hour period. See Warnings.
    • take a ½ teaspoon in a 4 fl. oz. (½ a glass) of water every 2 hours up to the maximum daily dosage or as directed by a doctor
    • dissolve completely in water before drinking
    agemaximum daily dosage
    adults 60 years of age and over½ teaspoon, 3 times a day
    adults under 60 and children 12 years of age and over½ teaspoon, 6 times a day
    children under 12 years of agedo not use

  • Other information

    • each ½ teaspoonful contains: sodium 716 mg
    • store in cool dry place below 77ºF
    • do not use if seal under cap is torn, broken or missing
  • INACTIVE INGREDIENT

    None

  • Questions & comments?

    PHARMADEL LLC.

    New Castle, DE, 19720

    +1-866-359-3478

    www.pharmadel.com

  • Prinicpal Display Panel

    55758-327-04

    4 Oz

    Rapidol SB 4 oz

  • INGREDIENTS AND APPEARANCE
    RAPIDOL SODIUM BICARBONATE 
    sodium bicarbonate powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55758-319
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM BICARBONATE (UNII: 8MDF5V39QO) (BICARBONATE ION - UNII:HN1ZRA3Q20) SODIUM BICARBONATE2.6 g  in 2.6 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55758-319-04113 g in 1 BOTTLE; Type 0: Not a Combination Product11/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33111/23/2020
    Labeler - Pharmadel LLC (030129680)
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