Label: TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin-b sulfate, pramoxine hydrochloride ointment

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 November 30, 2022

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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

  • Purpose

    First aid antibiotic

    Pain reliever

  • Uses

    First aid to help prevent infection and for the temporary relief of pain in minor

    • cuts 
    • scrapes 
    • burns
  • Warnings

    For external use only

    Do not use

    • if you are allergic to any of the ingredients
    • 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

    Stop use and ask a doctor if

    • you need to use for longer than one week
    • condition persists or gets worse
    • rash or other allergic reaction develops
    • symptoms persist for more than one week, or clear up and occur again with a few days

    Keep out of 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 older
      • clean the 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 15º-30ºC (59º-86ºF)
    • Before using any medication, read all label directions. Keep carton, it contains important information.
  • Inactive ingredient

    white petrolatum

  • Questions or comments?

    Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

  • Principal display panel

    Compare to Neosporin®+ Pain Relief active ingredients††

    Triple Antibiotic Ointment +

    Pain Relief

    BACITRACIN ZINC / NEOMYCIN

    SULFATE / POLYMYXIN BSULFATE /

    PRAMOXINE HCl

    FIRST AID ANTIBIOTIC /

    PAIN-RELIEVING OINTMENT

    TRIPLE ANTIBIOTIC

    MAXIMUM STRENGTH

    • First aid antibiotic
    • Pain-relieving ointment

    NET WT OZ (g)

    ††This product is not manufactured or distributed by Johnson & Johnson Corporation, owner f the registered trademark Neosporin® + Pain Relief

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

  • Package label

    Bacitracin zinc USP, 500 units, Neomycin 3.5 mg, Polymyxin B Sulfate USP, 10,000 units, Pramoxine Hydrochloride USP, 10 mg

    WALGREENS Triple Antibiotic Ointment Pain Relief

  • INGREDIENTS AND APPEARANCE
    TRIPLE ANTIBIOTIC 
    bacitracin zinc, neomycin sulfate, polymyxin-b sulfate, pramoxine hydrochloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2900
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [iU]  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:0363-2900-051 in 1 CARTON11/27/2020
    114 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333B11/27/2020
    Labeler - Walgreens (008965063)
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