Label: TRIPLE ANTIBIOTIC PLUS PAIN RELIEF MAXIMUM STRENGTH- bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride ointment

  • NDC Code(s): 68016-715-01
  • Packager: Chain Drug Consortium, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 6, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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

  • Purposes

    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 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 within 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 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 15°-30°C (59°-86°F)
    • 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

    + PAIN RELIEF

    Bacitracin Zinc • Neomycin Sulfate • Polymyxin B Sulfate • Pramoxine HCl

    Soothe Painful Cuts, Burns and Scrapes

    24 Hour Infection Protection

    Dual Action

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

    Distributed by:

    Pharmacy Value Alliance, LLC

    407 East Lancaster Avenue,

    Wayne, PA 19087

  • Package label

    Bacitracin zinc, USP 500 units, Neomycin 3.5 mg, Polymyxin B sulfate, USP 10,000 units, Pramoxine hydrochloride, USP 10 mg

    PREMIER VALUE Maximum Strength Triple Antibiotic + Pain Relief

  • INGREDIENTS AND APPEARANCE
    TRIPLE ANTIBIOTIC PLUS PAIN RELIEF  MAXIMUM STRENGTH
    bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-715
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [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 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:68016-715-011 in 1 CARTON07/10/2015
    128 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00407/10/2015
    Labeler - Chain Drug Consortium, LLC (101668460)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!