Label: PUBLIX BACITRACIN ZINC- bacitracin zinc ointment

  • NDC Code(s): 56062-815-28
  • Packager: PUBLIX SUPER MARKETS, INC.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 17, 2024

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

  • Drug Facts

  • Active ingredient

    Bacitracin Zinc 500 USP Units/gram 

  • Purpose 

    First aid antibiotic

  • Uses

    First aid to help prevent infection in minor:

    • cuts
    • scrapes
    • burns
  • Warnings 

    For external use only

    Allergy Alert 

    • do not use if you are allergic to any of the ingredients
  • When using this product 

    • do not use longer than 1 week
  • Do not use

    • in or near the eyes
    • on large areas of the body
  • Consult a doctor before use if you have;

    • deep or puncture wounds
    • animal bites
    • serious burns 
  • Stop use and consult a doctor if

    • condition persists or gets worse
    • symptoms last for more than 7 days or clear up and come back within a few days
    • a rash or other allergic reaction develops
  • Directions

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

    • Store at a controlled room temperature 20º-25ºC (68° to 77°F)
  • Inactive ingredient

    Petrolatum 

  • Principal display panel 

    Publix Bacitracin Zinc      56062-815-28

    First aid antibiotic ointment 

    NET WT 1 OZ (28g)

    Publix Bacitracin 1 oz Carton

    Publix Bacitracin 1 oz Tube

  • INGREDIENTS AND APPEARANCE
    PUBLIX BACITRACIN ZINC 
    bacitracin zinc ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:56062-815
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:56062-815-281 in 1 CARTON07/15/2024
    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 DrugM00407/15/2024
    Labeler - PUBLIX SUPER MARKETS, INC. (006922009)