Label: TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH- bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride ointment

  • NDC Code(s): 59779-823-34, 59779-823-56
  • Packager: CVS Pharmacy
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 9, 2023

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  • Drug Facts

  • Active ingredients (in each gram)

    Bacitracin zinc, USP 500 units
    Neomycin 3.5 mg
    Polymyxin B sulfate, USP 10,000 units
    Pramoxine hydrochloride, USP 10 mg

  • Purposes

    First aid antibiotic/Pain reliever

  • Uses

    First aid to help prevent infection and for temporary relief of pain or discomfort due to

    • minor cuts
    • scrapes
    • burns
  • Warnings

    For external use only

    Allergy alert:

    • do not use if allergic to any of the ingredients

    Do not use

    • in the eyes
    • over large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    When using this product

    • do not use longer than 1 week unless directed by a doctor

    Stop use and ask a doctor if

    • condition persists 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 right away.

  • Directions

    Adults and children 2 years of age and older:

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

    Children under 2 years of age: ask a doctor

  • Other information

    • Store at 59°-86°F (15°-30°C).
    • Before using any medication, read all label directions. Keep carton, it contains important information.
  • Inactive ingredient

    white petrolatum

  • Questions?

    1-800-432-8534 between 9 am and 4 pm EST, Monday-Friday.

  • PRINCIPAL DISPLAY PANEL

    CVSHealth™

    Compare to the active ingredients
    in Neosporin® + Pain Relief*

    NDC 59779-823-34

    Infection prevention for:
    • Burns
    • Cuts
    • Scrapes 

    MAXIMUM STRENGTH OINTMENT
    Triple Antibiotic & Pain Relief
    BACITRACIN ZINC–NEOMYCIN SULFATE-POLYMYXIN B SULFATE-PRAMOXINE HCl

    First aid antibiotic/pain relieving ointment

    NET WT 0.5 OZ (14 g)

    Triple Antibiotic & Pain Relief
  • INGREDIENTS AND APPEARANCE
    TRIPLE ANTIBIOTIC AND PAIN RELIEF  MAXIMUM STRENGTH
    bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-823
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10  mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-823-341 in 1 CARTON01/03/2005
    114 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:59779-823-561 in 1 CARTON01/03/2005
    228 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00401/03/200512/31/2024
    Labeler - CVS Pharmacy (062312574)
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