Label: WALGREENS BOIL PAIN RELIEF- boil pain relief ointment

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 12, 2024

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

View All Sections
  • Drug Facts 

  • Active Ingredient

    Benzocaine 20% 

  • Purpose 

    Pain Reliever 

  • Uses 

    • for the temporary relief of pain and discomfort casued by boils
  • WarningsFor 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 foreehead. 
  • When using this product 

    • avoid contact with eyes 
  • Stop use and ask a doctor if

    • fevers occur
    • redness around the bolis develops
    • condition worsens or does not improve
    • symptoms persist for mroe thna 3 days 
    • symptoms clear up and occur again within a few days. 
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of childern. If swallowed, get medical help

    or contact poison Control Center (1-800-222-1222) right away. 

  • Directions 

    • Adults and children 2 years and older; Apply to the affected areas not more than 2 times daily
    • Children under 2 years;ask a doctor
  • Other Information 

    Store as controlled room temperature 20-25 C ( 68-77F)

  • Inactive ingredients

    Beeswax, Camphor, Eucalyptus Oil, Lanolin, Menthol, Paraffin, Petrolatum, Thymol

  • Principal display panel 1 oz 

    Walgreens          NDC 0363-9095-28

    Boil Pain Relief Ointment 

    Benzocaine 20%/ Pain reliever

    NET WT 1 OZ (28g)

    280260 Tube

    580260 Carton

  • INGREDIENTS AND APPEARANCE
    WALGREENS BOIL PAIN RELIEF 
    boil pain relief ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9095
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE200 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    LANOLIN (UNII: 7EV65EAW6H)  
    MENTHOL (UNII: L7T10EIP3A)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    THYMOL (UNII: 3J50XA376E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9095-281 in 1 CARTON02/01/2024
    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 DrugM01702/01/2024
    Labeler - Walgreens Company (008965063)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!