Label: DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS PAIN RELIEF- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine ointment

  • NDC Code(s): 80489-857-01, 80489-857-02
  • Packager: OL PHARMA TECH, LLC Drs PHARMACY
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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  • Active ingredients

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

    Pramoxine hydrochloride 10 mg

  • Uses

    first aid to help prevent infection in minor
    • cuts
    • scrapes
    • burns

  • Purpose

    • first aid antibiotic
    • External Analgesic
  • Do Not Use

    Do not use
    • if you are allergic to any of the ingredients
    • in the eyes
    • over large areas of the body
    • longer than 1 week unless directed by a doctor

  • WARNINGS

    For external use only

  • ASK DOCTOR

    Ask a doctor before use if you have
    • deep or puncture wounds
    • animal bites
    • serious burns

  • STOP USE

    Stop use and ask a doctor if
    • the condition persists or gets worse
    • a rash or other allergic reaction develops

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    DIRECTIONS

    • 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

  • OTHER INFORMATION

    Store at room temperature

  • Inactive Ingredient

    Petrolatum

  • QUESTIONS

    www.drspharmacyusa.com

  • PRINCIPAL DISPLAY PANEL

    TRIPLE ANTIBIOTIC 2

  • INGREDIENTS AND APPEARANCE
    DRS. PHARMACY TRIPLE ANTIBIOTIC PLUS PAIN RELIEF 
    bacitracin zinc, neomycin sulfate, polymyxin b sulfate, lidocaine ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-857
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1000 mg
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1000 mg
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1000 mg
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80489-857-011 in 1 CARTON09/05/2021
    114000 mg in 1 TUBE; Type 0: Not a Combination Product
    2NDC:80489-857-021 in 1 CARTON09/05/2021
    228300 mg in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/05/2021
    Labeler - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
    Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
    Establishment
    NameAddressID/FEIBusiness Operations
    OL PHARMA TECH, LLC Drs PHARMACY021170377manufacture(80489-857)
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