Label: STOMACH RELIEF- bismuth subsalicylate tablet

  • 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 August 8, 2017

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

  • Active ingredient (in each caplet)

    Bismuth subsalicylate 262 mg

  • Purpose

    Upset stomach reliever and anti-diarrheal

  • KEEP OUT OF REACH OF CHILDREN

  • Uses

    relieves:

    • indigestion
    • nausea
    • heartburn
    • diarrhea
    • upset stomach associated with these symptoms
  • Warnings

    Reye's syndrome: Children and teenagers who have or are recovering from chicken 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
    • an ulcer
    • a bleeding problem

    Ask a doctor before use if you have

    • fever
    • mucus in the stool

    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 immediately.

  • Directions

    • Swallow caplet(s) with water, do not chew
    • adults and children 12 years and over: 2 caplets every 1/2 to 1 hour as needed
    • do not take more than 8 doses (16 caplets) in 24 hours
    • use untill diarrhea stops but not more than 2 days
    • children under 12 years: ask a doctor
    • drink plenty of fluids to help prevent dehydration which may accompany diarrhea.
  • Other information

    • each caplet contains: calcium 27 mg, salicylate 102 mg and sodium 2 mg.
    • very low sodium
    • TAMPER EVIDENT: Do not use if printed seal under cap is torn or missing.
    • store at room temperature, in a dry place
  • Inactive ingredients

    calcium carbonate, colloidal silicon dioxide, D and C red 27 lake, magnesium stearate, mannitol, microcrystalline cellulose, polysorbate 80, sodium starch glycolate.

  • PDP

    CVS Health

    Stomach Relief

    Bismuth Subsalicylate 262 mg

    Upset stomach reliever / Antidiarrheal

    Soothing relief for 5 symptoms:

    Heartburn

    Nausea

    Indigestion

    Diarrhea

    Upset Stomach

    Package contains One bottle

    24 Caplets

    BOX

  • INGREDIENTS AND APPEARANCE
    STOMACH RELIEF 
    bismuth subsalicylate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-172
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE262 mg
    Inactive Ingredients
    Ingredient NameStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    Product Characteristics
    ColorpinkScoreno score
    ShapecapsuleSize16mm
    FlavorImprint Code G172
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-172-121 in 1 CARTON03/04/2013
    124 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:69842-172-281 in 1 CARTON08/08/2011
    240 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33508/08/2011
    Labeler - CVS (062312574)