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

  • NDC Code(s): 11822-2700-1, 11822-2700-2, 11822-2700-5
  • Packager: Rite Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 13, 2024

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  • Drug Facts

  • Active ingredients (in each gram)

    Bacitracin Zinc USP, 500 units

    Neomycin 3.5 mg

    Polymyxin B sulfate USP, 10,000 units

    Pramoxine hydrochloride USP, 10 mg

  • Purpose

    First aid antibiotic

    Pain reliever

  • Uses

    First aid to help prevent infection and for the temporary relief of pain in minor

    • cuts 
    • scrapes 
    • burns
  • Warnings

    For external use only

    Do not use

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

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    Stop use and ask a doctor if

    • you need to use for longer than one week
    • condition persists or gets worse
    • rash or other allergic reaction develops
    • symptoms persist for more than one week, or clear up and occur again with a few days

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • adults and children 2 years of age and older
      • 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
    • children under 2 years of age: ask a doctor
  • Other information

    • Store at 15º-30ºC (59º-86ºF)
    • Before using any medication, read all label directions. Keep carton, it contains important information.
  • Inactive ingredient

    white petrolatum

  • Questions or comments?

    Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

  • Principal display panel

    Compare to the active ingredients in Neosporin® + Pain Relief Ointment*

    MAXIMUM STRENGTH

    TRIPLE ANTIBIOTIC OINTMENT + PAIN RELIEF

    BACITRACIN ZINC 

    NEOMYCIN SULFATE

    POLYMYXIN B SULFATE

    PRAMOXINE HCl

    FIRST AID ANTIBIOTIC /

    PAIN-RELIEVING OINTMENT

    FOR EXTERNAL USE ONLY

    HELP PREVENTINFECTION AND

    TEMPORARILY RELIEVES PAIN OF MINOR CUTS, SCRAPES, AND BURNS

    NET WT OZ (g)

    *This product is not manufactured or distributed by Johnson & Johnson Consumer, Inc distributor of Neosporin® + Pain Relief Ointment.

    DISTRIBUTED BY:

    RITE AID, 30 HUNTER LANE,

    CAMP HILL, PA 17011

    www.riteaid.com

  • Package label

    Bacitracin Zinc, USP 500 units, Neomycin 3.5 mg, Polymyxin B Sulfate, USP 10,000 units Pramoxine Hydrochloride, USP 10 mg

    RITE AID Maximum Strength Triple Antibiotic Ointment and Pain relief

  • INGREDIENTS AND APPEARANCE
    TRIPLE ANTIBIOTIC 
    bacitracin zinc, neomycin sulfate, polymyxin-b sulfate, pramoxine hydrochloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-2700
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [iU]  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 B10000 [USP'U]  in 1 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE10 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-2700-51 in 1 CARTON02/25/2022
    114 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:11822-2700-11 in 1 CARTON02/25/2022
    228 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:11822-2700-22 in 1 CARTON02/25/2022
    328 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00402/25/2022
    Labeler - Rite Aid Corporation (014578892)
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