Label: DABUR FIRST AID- bacitracin zinc ointment

  • NDC Code(s): 68747-3035-2, 68747-3035-3, 68747-3035-4, 68747-3035-5, view more
    68747-3035-6
  • Packager: Dabur India Limited
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 16, 2024

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

View All Sections
  • Active Ingredient (in each gram)

    Bacitracin Zinc (equal to 500 bacitracin 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

    ■ Not for opthalmic use Do not use■ in the eyes ■ if you are allergic to any of the ingredients ■ 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 ■ serious burns

  • Stop use and ask a doctor if

    ■ the condition persists or gets worse

    ■ a rash or other allergic reaction develops

  • Keep out of reach of children

    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

    ■ store at room temperature 15-30C (59-86F)

    ■ avoid excessive heat and humidity

  • Inactive Ingredients

    hard paraffin, liquid paraffin, white soft paraffin, lanolin

  • Package Label

    Package Label

  • INGREDIENTS AND APPEARANCE
    DABUR  FIRST AID
    bacitracin zinc ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68747-3035
    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
    PARAFFIN (UNII: I9O0E3H2ZE)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    LANOLIN (UNII: 7EV65EAW6H)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68747-3035-20.9 g in 1 PACKET; Type 0: Not a Combination Product05/30/2013
    2NDC:68747-3035-314 g in 1 TUBE; Type 0: Not a Combination Product05/30/2013
    3NDC:68747-3035-428 g in 1 TUBE; Type 0: Not a Combination Product05/30/2013
    4NDC:68747-3035-5113 g in 1 TUBE; Type 0: Not a Combination Product05/30/2013
    5NDC:68747-3035-6425 g in 1 JAR; Type 0: Not a Combination Product05/30/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00405/30/2013
    Labeler - Dabur India Limited (650319218)
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!