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Bacitracin (Dynarex Corporation)

Available Formats

Dosage Form Package Information Links
OINTMENT 12 BOX in 1 CASE (67777-219-07) > 144 PACKET in 1 BOX > .9 g in 1 PACKET Label Information
OINTMENT 72 TUBE in 1 CASE (67777-219-05) > 56.7 g in 1 TUBE Label Information
OINTMENT 72 TUBE in 1 CASE (67777-219-01) > 28.35 g in 1 TUBE Label Information
OINTMENT 72 TUBE in 1 CASE (67777-219-02) > 113.4 g in 1 TUBE Label Information
OINTMENT 12 JAR in 1 CASE (67777-219-03) > 425.3 g in 1 JAR Label Information
OINTMENT 72 TUBE in 1 CASE (67777-219-04) > 14.17 g in 1 TUBE Label Information
OINTMENT 12 BOX in 1 CASE (67777-219-06) > 144 PACKET in 1 BOX > .5 g in 1 PACKET Label Information

Complete Bacitracin Information

  • ACTIVE INGREDIENT

    Active ingredient               Purpose
    Bacitracin 500 Units                Antibiotic


  • Warnings:

    For external use only

    Dosage and Administration:
    • clean the affected areas
    • apply a small amount of 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

    Stop use and ask a doctor if
    •  the condition persists or gets worse, or if a rash or other allergic reaction develops.

    Do not use:
    • if you are allergic to any of the ingredients
    • in the eyes
    • over large areas of the body
    • longer than 1 week unless directed by a doctor

    Keep out of reach of children

    if swallowed, get medical help or contact a Poison Control Center right away


  • Purpose

    First aid to help prevent infection in:
    Minor cuts
    scrapes
    burns


  • Indications and Usage

    Ask a doctor before use:

    • in case of deep or puncture wounds
    • animal bites
    • serious burns


  • Other information

    • store at controlled room temperature 15°-30° C (59°-86° F)

  • Inactive ingredients

    Light Mineral Oil, White Petrolatum


  • Principal Display Panel

    Bacitracin Ointment:

    bacitracin-galentic-ointment-01.jpg

    1162_1163_Bacitracin_Ointment


  • INGREDIENTS AND APPEARANCE
    BACITRACIN 
    bacitracin ointment
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-219
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [iU]  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:67777-219-01 72 in 1 CASE
    1 28.35 g in 1 TUBE
    2 NDC:67777-219-04 72 in 1 CASE
    2 14.17 g in 1 TUBE
    3 NDC:67777-219-06 12 in 1 CASE
    3 144 in 1 BOX
    3 0.5 g in 1 PACKET
    4 NDC:67777-219-07 12 in 1 CASE
    4 144 in 1 BOX
    4 0.9 g in 1 PACKET
    5 NDC:67777-219-05 72 in 1 CASE
    5 56.7 g in 1 TUBE
    6 NDC:67777-219-02 72 in 1 CASE
    6 113.4 g in 1 TUBE
    7 NDC:67777-219-03 12 in 1 CASE
    7 425.3 g in 1 JAR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part333B 12/01/2009
    Labeler - Dynarex Corporation (008124539)
    Registrant - Dynarex Corporation (008124539)