Label: ANBESOL MAXIMUM STRENGTH- benzocaine solution

  • NDC Code(s): 80070-230-41
  • Packager: Foundation Consumer Brands
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 6, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Benzocaine 20%

  • Purpose

    Oral pain reliever

  • Uses

    • temporarily relieves pain associated with the following mouth and gum irritations:
      • toothache
      • sore gums
      • canker sores
      • braces
      • minor dental procedures
      • dentures
  • Warnings

    METHEMOGLOBINEMIA WARNING

    Use of this product may cause methemoglobinemia, a rare but serious condition that must be treated promptly because it reduces the amount of oxygen carried in blood. This can occur even if you have used this product before. Stop use and seek immediate medical attention if you or a child in your care develops:

    • pale, gray, or blue colored skin (cyanosis)
    • headache
    • rapid heart rate
    • shortness of breath
    • dizziness or lightheadedness
    • fatigue or lack of energy

    Allergy alert

    Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics.

    Do not use

    • for teething
    • in children under 2 years of age

    When using this product

    • avoid contact with the eyes
    • do not exceed recommended dosage
    • do not use for more than 7 days unless directed by a doctor/dentist

    Stop use and ask a doctor if

    • sore mouth symptoms do not improve in 7 days
    • irritation, pain, or redness lasts or worsens
    • swelling, rash, or fever develops

    Keep out of reach of children.If more than used for pain is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    adults and children 2 years of age and overwipe liquid on with cotton, or cotton swab, or fingertip, apply to the affected area up to 4 times daily or as directed by a doctor/dentist
    children under 12 years of ageadult supervision should be given in the use of this product
    children under 2 years of agedo not use
    • for denture irritation:
      • apply thin layer to the affected area
      • do not reinsert dental work until irritation/pain is relieved
      • rinse mouth well before reinserting
  • Other information

    store at 20-25°C (68-77°F)

  • Inactive ingredients

    benzyl alcohol, D&C yellow no. 10, FD&C blue no. 1, FD&C red no. 40, methylparaben, natural flavor, polyethylene glycol, polysorbate 80, propylene glycol, saccharin

  • Questions or comments?

    Call 1-888-594-0673weekdays 9 AM to 5 PM EST

  • SPL UNCLASSIFIED SECTION

    Distributed by: Foundation Consumer Brands, LLC
    Pittsburgh, PA 15212

  • PRINCIPAL DISPLAY PANEL - 12 mL Bottle Blister Pack

    MAXIMUM STRENGTH

    20% Benzocaine

    Anbesol ®

    Oral Pain Reliever/Benzocaine 20%

    Instant Oral
    Pain Relief

    ADA Accepted

    American Dental Association

    • Toothaches
    • Canker Sores
    • Aligner Pain
    • Gum Pain

    LIQUID

    0.41 FL OZ (12 mL)

    anbesol label

  • INGREDIENTS AND APPEARANCE
    ANBESOL  MAXIMUM STRENGTH
    benzocaine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80070-230
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SACCHARIN (UNII: FST467XS7D)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80070-230-411 in 1 BLISTER PACK09/15/2021
    112 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02209/15/2021
    Labeler - Foundation Consumer Brands (117603632)
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