Label: TRIPLE ANTIBIOTIC swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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 December 15, 2020

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  • Active Ingredients

    (in each gram)

    Bacitracin zinc 400 units

    Neomycin sulfate (3.5mg Neomycin)

    Polymyxin B sulfate 5000 units

  • Purpose

    Antibiotics

  • Use

    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

    • 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 and ask a doctor:

    • a rash or allergic reation develops
    • condition worsens or persists
  • Keep out of reach of children.

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

  • Directions

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

    petrolatum

  • RapidCare - Triple Antibiotic Towelettte - 1pc

    Triple Antibiotic

  • INGREDIENTS AND APPEARANCE
    TRIPLE ANTIBIOTIC 
    triple antibiotic swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73659-005
    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:73659-005-100.5 g in 1 PACKET; Type 0: Not a Combination Product04/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333B04/01/2020
    Labeler - Rapid Care, Inc (877432778)
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