Label: MEDICHOICE BACITRACIN- bacitracin ointment

  • NDC Code(s): 39892-0810-1, 39892-0810-3
  • Packager: Owens & Minor, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 9, 2023

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

View All Sections
  • Drug Facts

  • Active Ingredient (In Each Gram)

    Bacitracin 500 units

    Purpose

    First aid antibiotic

  • Uses

    First aid to help prevent infection in: • minor cuts • scrapes • burns

  • Warnings

    • for external use only

    Do not use:

    • in the eyes • if you are allergic to any of the ingredients, due to the possibility of anaphylactic shock • over large areas of the body • longer than 1 week unless directed by a doctor


    Stop use and ask a doctor:

    • before use in case of deep puncture wounds, animal bites or serious burns • if the condition persists or gets worse • if a rash or other allergic reaction develops

    KEEP OUT OF REACH OF CHILDREN.

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

  • Other Information:

    • Tamper Evident. Do not use if package is torn, cut or opened. • Avoid excessive heat and humidity • Store at a controlled room temperature 15˚ to 30˚C (59˚ to 86˚F)

  • Inactive Ingredients

    white petrolatum.

  • Product Labels

    12

  • INGREDIENTS AND APPEARANCE
    MEDICHOICE BACITRACIN 
    bacitracin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39892-0810
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [iU]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:39892-0810-31 in 1 CARTON03/26/201505/31/2017
    128.35 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:39892-0810-1144 in 1 BOX03/26/2015
    20.9 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00403/26/2015
    Labeler - Owens & Minor, Inc (847412269)
    Registrant - Owens & Minor, Inc (847412269)
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!