Label: PROCUREFIRST AID ANTIBIO FIRST AID ANTIBIOTIC- bacitracin ointment

  • NDC Code(s): 55681-218-01, 55681-218-02
  • Packager: TWIN MED, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 8, 2024

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  • Active Ingredients(in each gram)

    Bacitracin Zinc (equal to 500 Bacitracin units)


  • Purpose

    Antibiotic

  • Uses

    First aid to prevent infection in Minor cuts, Scrapes & Burns

  • Directions

    • Clean the affected area
    • Apply small amount of this product(an amount equal to the surface area of the tip of the finger) on the area 1 to 3 times daily
    • May be covered with a sterile bandage
  • Warnings

    For External Use Only.

    Do not use

    • In the eyes
    • If you are allergic to any of the ingredients, due to possibility of anaphylactic shock
    • Over large areas of the body
    • Longer than 1 week unless directed by a doctor
    • Ask a doctor before use in case of deep or puncture wounds, animal bites or serious burns

    Stop use and ask a doctor if

    • The condition persists or gets worse
    • A rash or allergic reaction develops

    Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Centre right away

    Other information

    • Store at controlled room temperature 15 o - 30 oC(59 o--86 o F)
    • Avoid excessive heat and humidity
    • Tamper Evident
    • Do not use if packet is torn, cut, or opened.

    Inactive Ingredients

    Hard Paraffin, Lanolin, Liquid Paraffin,White Soft Paraffin

  • Principal Display Panel

    Drug Fact and PDP

  • INGREDIENTS AND APPEARANCE
    PROCUREFIRST AID ANTIBIO  FIRST AID ANTIBIOTIC
    bacitracin ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55681-218
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 U  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PARAFFIN (UNII: I9O0E3H2ZE)  
    LANOLIN (UNII: 7EV65EAW6H)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55681-218-010.9 g in 1 PACKET; Type 0: Not a Combination Product09/22/2021
    2NDC:55681-218-0228.3 g in 1 TUBE; Type 0: Not a Combination Product08/18/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00402/05/2013
    Labeler - TWIN MED, LLC (009579330)
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