Label: TRIPLE ANTIBIOTIC AND PAIN RELIEF- triple antibiotic ointment

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

Drug Label Information

Updated January 17, 2024

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  • Drug Facts 

  • Active ingredients (in each gram)

    Bacitracin 500

    Neomycin 3.5 mg

    Polymyxin B 10,000 units

    Pramoxine HCL 10 mg

  • Purpose

    First aid antibiotic

    First aid antibiotic

    First aid antibiotic

    Pain Relief

  • Uses

    helps prevent infection in and temporarily relieves pain due to minor:

    • cuts
    • scrapes
    • burns
  • WarningsFor external use only 

    Do not use

    • do not use if you are allergic to any of the ingredients
    • or near the eyes
    • or 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 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

    Keep out of the reach of children. If swallowed get medical help or contact a Poison Control Center immediately.

  • Directions

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

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

  • Inactive ingredient

    Petrolatum 

  • Questions or comments? 1-800-910-6874

  • Principal Display panel 

    Target Up & Up    NDC 11673-746-28

    Maximum Strength Pain Relieving 

    First aid Antibiotic Ointment 

    Polymixin B Sulfate/Bacitracin Zinc/Neomycin Sulfate/ Pramoxine HCl

    NET WT 1.0 OZ (28g)

    291001 Tube

    591001 Carton

  • INGREDIENTS AND APPEARANCE
    TRIPLE ANTIBIOTIC AND PAIN RELIEF 
    triple antibiotic ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-746
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  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:11673-746-281 in 1 CARTON01/31/2024
    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 DrugM00401/31/2024
    Labeler - Target Corporation (006961700)
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