Label: BOIL EASE- benzocaine ointment

  • NDC Code(s): 63736-040-28
  • Packager: Insight Pharmaceuticals LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 10, 2020

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  • SPL UNCLASSIFIED SECTION

    BOIL EASE® 
    PAIN RELIEVING OINTMENT

    Drug Facts

  • Active ingredient

    Benzocaine 20%

  • Purpose

    Pain Reliever

  • Use

    for the temporary relief of pain and discomfort caused by boils

  • Warning

    For external use only

    Do not use

    for more than 3 days

    Ask a doctor before use if you have

    boils on the lips, nose, cheeks, or forehead

    When using this product

    avoid contact with the eyes

    Stop use and ask a doctor if

    • fever occurs
    • redness around the boil develops
    • condition worsens or does not improve
    • symptoms persist for more than 3 days
    • symptoms clear up and occur again within a few days

    Keep out of the reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    Adults and children 2 years of age and olderApply to affected area no more than 2 times daily
    Children under 2 years of ageConsult a doctor
  • Other information

    Keep carton for full drug facts

  • Inactive ingredients

    anhydrous lanolin, camphor, eucalyptus oil, menthol, petrolatum, thymol, yellow wax

  • Questions?

    call 1-800-344-7239

  • PRINCIPAL DISPLAY PANEL

    28 g Tube Carton
    BOIL EASE® 
    PAIN RELIEVING OINTMENT
    BENZOCAINE 20%
    NET WT 1 oz (28 g)

    PRINCIPAL DISPLAY PANEL 28 g Tube Carton BOIL EASE® PAIN RELIEVING OINTMENT BENZOCAINE 20% NET WT 1 oz (28 g)

  • INGREDIENTS AND APPEARANCE
    BOIL EASE 
    benzocaine ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63736-040
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LANOLIN (UNII: 7EV65EAW6H)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    MENTHOL (UNII: L7T10EIP3A)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    THYMOL (UNII: 3J50XA376E)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    Product Characteristics
    ColorYELLOWScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63736-040-281 in 1 BOX06/21/2010
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34806/21/2010
    Labeler - Insight Pharmaceuticals LLC (055665422)
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