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

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated June 14, 2024

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  • Drug Facts

  • Active ingredients & Purpose

    Active ingredients Purpose
    Bacitracin zinc 400 units ..................First aid antibiotic
    Neomycin sulfate 3.5 mg..................First aid antibiotic
    Polymyxin B sulfate 5,000 units .......First aid antibiotic
  • Uses

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

  • Warnings

    For external use only.

    Do not use

    • in the eyes
    • over large areas of the body
    • if you are allergic to any of the ingredients

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • condition persists or gets worse
    • a rash or other allergic reaction develops
    • you need to use longer than 1 week

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    • clean the affected area
    • apply a small amount of this product (an amount equal to the surface of the tip of a finger) on the area 1 to 3 times daily
    • may be covered with a sterile bandage
  • Other information

    • store between (68-77°F) 20-25°C
    • don’t use if foil seal under cap is punctured, torn, or missing
  • Inactive ingredients

    cocoa butter, cottonseed oil, mineral oil, olive oil, paraffin, sodium pyruvate, tocopherol acetate (vit. E), white petrolatum

  • Principal Display Panel

    Rapidol Triple PDP

  • INGREDIENTS AND APPEARANCE
    RAPIDOL  TRIPLE ANTIBIOTIC
    bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55758-440
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    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
    POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PARAFFIN (UNII: I9O0E3H2ZE)  
    COTTONSEED OIL (UNII: H3E878020N)  
    COCOA BUTTER (UNII: 512OYT1CRR)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    SODIUM PYRUVATE (UNII: POD38AIF08)  
    WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
    Product Characteristics
    Colorwhite (Translucent) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55758-440-021 in 1 CARTON06/30/2024
    156 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00406/30/2024
    Labeler - Pharmadel LLC (030129680)
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