Label: EQUALINE MAXIMUM STRENGTH STOMACH RELIEF- bismuth subsalicylate liquid

  • NDC Code(s): 41163-937-04, 41163-937-05
  • Packager: Supervalu Inc.
  • 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 January 11, 2022

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

  • ACTIVE INGREDIENT(in each 30 mL)

    Bismuth subsalicylate 1050 mg

  • PURPOSE

    Upset stomach reliever and anti-diarrheal

  • USE(S)

    relieves:


    • diarrhea
    • heartburn
    • indigestion
    • nausea
    • 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

    • an ulcer
    • bloody or black stool
    • 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 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

    • shake well before use
    • mL = milliliter
    • TBSP = tablespoon
    • adults and children 12 years and over: 1 dose (2 TBSP or 30 mL) every hour as needed
    • do not exceed 4 doses (8 TBSP or 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 fluids to help prevent dehydration caused by diarrhea
  • OTHER INFORMATION

    • each 30 mL or 2 TBSP contains:
    • potassium 25 mg
    • salicylate 471 mg
    • sodium 8 mg
    • protect from freezing
    • avoid excessive heat (over 104oF or 40oC)
    • dosage cup provided
  • INACTIVE INGREDIENTS

    benzoic acid, D&C red # 22, D&C red # 28, flavor, hydroxyethyl cellulose, potassium hydroxide, purified water, saccharin sodium, salicylic acid, simethicone, xanthan gum

  • PRINCIPAL DISPLAY PANEL

    NDC 41163-937-05
    compate to Pepto-Bismol Maximum Strength active ingredient*
    EQUALINE
    maximum strength
    stomach relief liquid
    bismuth subsalicylate 1050 mg per 30 mL
    (upset stomach reliever/antidiarrheal)

    5 symptom digestive relief:


    • heartburn
    • indigestion
    • nausea
    • upset stomach
    • diarrhea

    12 FL OZ (354 mL)


    47


  • INGREDIENTS AND APPEARANCE
    EQUALINE MAXIMUM STRENGTH STOMACH RELIEF 
    bismuth subsalicylate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-937
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BISMUTH SUBSALICYLATE (UNII: 62TEY51RR1) (SALICYLIC ACID - UNII:O414PZ4LPZ) BISMUTH SUBSALICYLATE1050 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    D&C RED NO. 22 (UNII: 1678RKX8RT)  
    D&C RED NO. 28 (UNII: 767IP0Y5NH)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorPINKScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-937-05354 mL in 1 BOTTLE; Type 0: Not a Combination Product09/23/2018
    2NDC:41163-937-04237 mL in 1 BOTTLE; Type 0: Not a Combination Product09/23/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart33509/23/2018
    Labeler - Supervalu Inc. (006961411)