Label: DRS PHARMACY TRIPLE ANTIBIOTIC PAIN PLUS ITCH PLUS SCAR- bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment ointment

  • NDC Code(s): 80489-412-01, 80489-412-02
  • Packager: OL PHARMA TECH, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

If you are a consumer or patient please visit this version.

  • Active Ingredients

    • Bacitracin Zinc 500 units
    • Neomycin Sulfate 3.5mg
    • Polymyxin B Sulfate 10,000 units
    • pramoxine HCL 10mg
  • Purpose

    • First aid antibiotic
  • Uses

    First aid to help prevent infection in minor:

    • cuts
    • scrapes
    • burns
  • Warnings

    For external use only

  • Ask a doctor

    Ask a doctor before use if you have

    • serious burns
    • deep or puncture wounds
    • animal bites
  • Stop use and ask a doctor

    Stop use and ask a doctor if

    • condition persists or gets worse
    • rash or other allergic reaction develops
  • Do not use

    • do not use in the eyes
    • do not apply over large areas of the body
    • if you are allergic to any of the ingredients
    • longer than one week unless directed by your doctor
  • keep out of the reach of children

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

  • Directions

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

    • store at room temperature
  • Inactive ingredient

    Petrolatum

  • Questions

    www.drspharmacyusa.com

  • Principal display panel

    TRIPLE ANTIBIOTIC

  • INGREDIENTS AND APPEARANCE
    DRS PHARMACY TRIPLE ANTIBIOTIC PAIN PLUS ITCH PLUS SCAR 
    bacitracin zinc, polymyxin b sulfate, neomycin sulfate ointment ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80489-412
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC500 [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)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80489-412-011 in 1 CARTON02/16/2021
    114 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:80489-412-021 in 1 CARTON02/16/2021
    228.3 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/16/2021
    Labeler - OL PHARMA TECH, LLC (021170377)
    Registrant - OL PHARMA TECH, LLC Drs PHARMACY (021170377)
    Establishment
    NameAddressID/FEIBusiness Operations
    OL PHARMA TECH, LLC Drs PHARMACY021170377manufacture(80489-412)