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

  • NDC Code(s): 75568-015-01
  • Packager: Planet (Anhui) Pharmaceutical Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2023

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  • Drug Facts

  • Active Ingredients

    (in each gram) Bacitracin zinc (400 units Bacitracin) Neomycin sulfate (3.5mg Neomycin) Polymyxin B sulfate (Polymyxin B 5000 units)

    Purpose

    First aid Antibiotic

  • Uses

    first aid to help prevent infection in minor scrapes, cuts, and burns

  • Warnings

    For external use only

    Do not use

    • internally • in eyes • over large areas of the body or on puncture wounds, animals bites or serious burns • for more than one week unless directed by a doctor • if you are allergic to any of the ingredients

    Stop use and ask a doctor if

    • a rash or allergic reaction develops

    • condition worsens or persists

    Keep out of reach of children

    if ingested contact a Poison Control Center right away

  • Directions

    • clean affected area • apply a small amount 1 to 3 times daily • may cover with a sterile bandage

  • Inactive Ingredients

    petrolatum

  • Questions?

    1-888-655-1558

  • Package Labeling:

    Label0

  • INGREDIENTS AND APPEARANCE
    CARELAND TRIPLE ANTIBIOTIC 
    bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75568-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [CFU]  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 B5000 [CFU]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75568-015-010.9 g in 1 BAG; Type 0: Not a Combination Product10/30/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00410/30/2023
    Labeler - Planet (Anhui) Pharmaceutical Co., Ltd. (618456104)
    Establishment
    NameAddressID/FEIBusiness Operations
    Planet (Anhui) Pharmaceutical Co., Ltd.618456104manufacture(75568-015)
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