Label: GOOD NEIGHBOR ULTRA STRENGTH STOMACH RELIEF- bismuth subsalicylate suspension

  • 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 February 8, 2023

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

  • Active ingredient (in each 15 mL dose)

    Bismuth subsalicylate 525 mg

  • Purposes

    Upset stomach reliever and antidiarrheal

  • Uses

    relieves

    travelers’ diarrhea
    diarrhea
    upset stomach due to overindulgence in food and drink, including:
    heartburn
    indigestion
    nausea
    gas
    belching
    fullness
  • 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 or 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

    an ulcer
    a bleeding problem
    bloody or black stool

    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 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 or last more than 2 days
    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 at (1-800-222-1222).

  • Directions

    shake well before use
    only use dose cup provided
    adults and children 12 years and over: 15 mL (1 dose) every 1/2 or 30 mL (2 doses) every hour as needed for diarrhea/traveler’s diarrhea.
    15 mL (1 dose) every 1/2 hour as needed for overindulgence (upset stomach, heartburn, indigestion, nausea)
    do not exceed 8 doses (120 mL) in 24 hours
    use until diarrhea stops but not more than 2 days
    children under 12 years: ask a doctor
    drink plenty of clear fluids to help prevent dehydration caused by diarrhea
  • Other information

    each 15 mL contains: sodium 10 mg
    salicylate 230 mg
    low sodium
    sugar free
    store at room temperature
    protect from freezing
    avoid excessive heat (over 104°F or 40°C)
  • Inactive ingredients

    carboxymethylcellulose sodium, D&C Red No. 22, D&C Red No. 28, flavor, microcrystalline cellulose, potassium hydroxide, potassium sorbate, purified water, salicylic acid, simethicone emulsion, sodium benzoate, sucralose, xanthan gum

  • Questions or comments?

    1-866-467-2748

    DO NOT USE IF IMPRINTED SHRINK BAND IS MISSING OR BROKEN.

  • Principal Display Panel

    GOOD NEIGHBOR PHARMACY®

    Compare to PEPTO-BISMOL® Ultra Strength active ingredient*

    Pink Bismuth

    Ultra-Strength

    Bismuth Subsalicylate

    Upset Stomach Reliever & Anti-diarrheal

    Relieves Upset Stomach, Nausea, Heartburn Indigestion & Diarrhea

    Original Flavor

    Distributed by:

    AmerisourceBergen

    1 West First Avenue

    Conshohocken PA 19428

    Questions or Concerns?

    www.mygnp.com

    *This product is not manufactured or distributed by PROCTER & GAMBLE INC., distributor of PEPTO-BISMOL® Ultra Strength

    Good NeighborUltra Strength Stomach Relief
  • INGREDIENTS AND APPEARANCE
    GOOD NEIGHBOR ULTRA STRENGTH  STOMACH RELIEF
    bismuth subsalicylate suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46122-747
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (BISMUTH CATION - UNII:ZS9CD1I8YE, SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE525 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    D&C RED NO. 22 (UNII: 1678RKX8RT)  
    D&C RED NO. 28 (UNII: 767IP0Y5NH)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:46122-747-06236 mL in 1 BOTTLE; Type 0: Not a Combination Product01/23/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33501/23/2023
    Labeler - AMERISOURCE BERGEN (007914906)