Label: CURAD MAXIMUM STRENGTH TRIPLE ANTIBIOTIC- bacitracin, neomycin, polymyxin b, pramoxine hydrochloride ointment

  • NDC Code(s): 53329-031-01
  • Packager: Medline Industries, LP
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 1, 2025

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  • Active ingredients (in each gram)

    Bacitracin 500 units

    Neomycin 3.5 mg

    Polymyxin B 10,000 units

    Pramoxin hydrochloride 10 mg

  • Purposes

    First aid antibiotic

    First aid antibiotic

    First aid antibiotic

    Pain reliever

  • Uses

    • First aid to help prevent infection in and temporarily relieves pain due to
    • minor cuts
    • scrapes
    • burns
  • Warnings

    • For external use only

    Do not use

    • if allergic to any of the ingredients
    • in or near the eyes
    • on large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • you need to use longer than 1 week
    • condition lasts or gets worse
    • symptoms last for more than 7 days, or clear up and come back within a few days
    • a rash or other allergic reaction develops

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    Adults and children 2 years and older:

    • clean affected area
    • apply a small amount (equal to the surface area of tip of finger) on area 1 to 3 times daily
    • may be covered with a sterile bandage.

    Children under 2 years: ask a doctor

  • Other information

    Store at controlled room temperature 68º-77ºF (20º-25ºC).

  • Inactive ingredient

    petrolatum

  • Manufacturing Information

    Manufactured for:

    Medline Industries, LP

    Three Lakes Drive Northfield, IL 60093 USA


    www.curad.com

    1-800-MEDLINE (633-5463)

    REF: CUR001232

  • Package Label

    label

  • INGREDIENTS AND APPEARANCE
    CURAD MAXIMUM STRENGTH TRIPLE ANTIBIOTIC 
    bacitracin, neomycin, polymyxin b, pramoxine hydrochloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-031
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC500 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53329-031-011 in 1 BOX12/01/2019
    128.4 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00412/01/2019
    Labeler - Medline Industries, LP (025460908)
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