Label: TRIPLE ANTIBIOTIC ointment

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 14, 2021

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  • Active Ingredients

    (in each gram)

    Bacitracin Zinc (400 units Bacitracin)

    Neomycin Sulfate (3.5mg Neomycin)

    Polymyxin B Sulfate (Polymyxin B 5000 units)

  • Purpose

    Antibiotics

  • Uses

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

  • Warnings

    For external use only

  • Flamable, keep away from fire or flame

  • Do Not Use

    • in the eyes
    • internally
    • over large areas of the body
    • if you are allergic to any of the ingredients
    • longer than 1 week unless directed by a doctor
  • Stop use and ask a doctor:

    • the condition persists or gets worse
    • a rash or other allergic reaction develops
  • Keep out of reach of children.

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

  • 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
  • Inactive ingredient

    petrolatum

  • RapidCare - Triple Antibiotic Towelettte - 1pc

    Triple Antibiotic

  • INGREDIENTS AND APPEARANCE
    TRIPLE ANTIBIOTIC 
    triple antibiotic ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73659-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [USP'U]  in 1 g
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 [USP'U]  in 1 g
    NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN3.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73659-010-100.5 g in 1 PACKET; Type 0: Not a Combination Product12/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333B12/15/2020
    Labeler - Rapid Care, Inc (877432778)
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