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

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

Drug Label Information

Updated March 19, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    (in each gram)

    Bacitracin zinc 400 units

    Neomycin sulfate (3.5 mg Neomycin) Polymyxin B sulfate 5000 units

  • Purpose

    First Aid

    Antibiotics

  • Uses

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

  • Warnings

    External use only.

    Do not use

    • internally
    • in eyes
    • over large areas of the body or on puncture wounds, animal bites or serious burns
    • for more than 1 week unless directed by a doctor
    • if you are allergic to any of the ingredients

    Stop use, ask a doctor

    • a rash or allergic reactions 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

    Welly Health PBC, Minn., MN 55402

    1-833-BE-WELLY

  • Principal Display Panel - Antibiotic Pouch Label

    Welly™

    Triple Antibiotic
    Ointment

    0.5g/ 1/57 OZ

    Principal Display Panel - Antibiotic Pouch Label
  • INGREDIENTS AND APPEARANCE
    ANTIBIOTIC 
    bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72663-560
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN6 mg  in 1 mL
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE3.5 mg  in 1 mL
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B0.77 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72663-560-340.5 mL in 1 POUCH; Type 0: Not a Combination Product02/25/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00402/25/2019
    Labeler - Welly Health PBC (116766884)
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