Label: BISMUTH- bismuth subsalicylate liquid

  • 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 April 30, 2018

If you are a consumer or patient please visit this version.

  • Active ingredient (in each tablespoon= 15 mL)

    Bismuth subsalicylate 262 mg

  • Purpose

    Upset stomach reliever and anti-diarrheal

  • Uses

    • relieves upset stomach due to overindulgence in food or drink
    • controls diarrhea
  • Warnings

    Reye's syndrome: Children and teenagers who have or are recovering from children pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye's syndrome, a rare but serious illness.

    Allergy alert:  Contains salicylate. Do not take  if you are

    • allergic to salicylates (including aspirin)
    • taking other salicylate products

    Do not use

    • if you have bloody or black stool
    • if you have an ulcer or bleeding problem

    Ask a doctor before use if you have

    • fever
    • mucus in the stool
    • a magnesium-restricted diet
    • a sodium-restricted diet

    Ask a doctor or pharmacist before use if you are

    • taking any drug for
    • anticoagulation (thinning of the blood)
    • diabetes
    • gout
    • arthritis

    When using this product

    a temporary but harmless, darkening of the stool and/or tongue may occur

    Stop use and ask a doctor if

    • symptoms get worse
    • ringing in the ears or loss of hearing occurs
    • diarrhea lasts more than 2 days

    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

    • drink plenty of clear fluids to help prevent dehydration caused by diarrhea
    • shake well before using
    • use pre-measured cup for accurate dosing
    • repeat dosage every 1/2 to 1 hour as needed
    • do not take more than 8 doses in 24 hours
    • use until diarrhea stops but not more than 2 days
    • adults & children 12 years and over: 2 tablespoons
    • children under 12 years: ask a doctor
  • Inactive ingredients

    Carboxymethylcellulose sodium, D&C Red #3, FD&C Red #40, flavor, glycerin, magnesium aluminum silicate, saccharin sodium, salicylic acid, sodium benzoate, sodium saliycylate, sorbitol, water

  • STORAGE AND HANDLING

    • Store at room temperature. Protect from freezing and excessive heat (over 40oF or 104oC)
    • each tablespoon (15 mL) contains: magnesium 32 mg
    • each tablespoon (15 mL) contains: sodium 24 mg
    • each tablespoon (15 mL) contains: total salycylate 159 mg
    • TAMPER EVIDENT:Do not use if printed inner cap seal is broken or missing..
  • Principal Display Panel

    Bismuth label

  • INGREDIENTS AND APPEARANCE
    BISMUTH  
    bismuth subsalicylate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53807-152
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE) BISMUTH SUBSALICYLATE262 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    FD&C RED NO. 3 (UNII: PN2ZH5LOQY)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM SALICYLATE (UNII: WIQ1H85SYP)  
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorpinkScore    
    ShapeSize
    FlavorPEPPERMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53807-152-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product03/16/1999
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33503/16/1999
    Labeler - Rij Pharmaceutical Corporation (144679156)
    Establishment
    NameAddressID/FEIBusiness Operations
    Rij Pharmaceutical Corporation144679156manufacture(53807-152)