Label: BENZOIN swab

  • NDC Code(s): 46414-8888-2
  • Packager: James Alexander Corporation
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 27, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Drug Facts

  • Active Ingredients (each swab)

    Benzoin 10%}

    Aloe 2%} 

    Storax 8%}

    Tolu Balsam 4%}

  • Purpose

    Topical bandage adhesive

  • Uses

    An adhesive to hold bandages in place.

  • Warnings

    For external use only.

    Allergy alert if you have had a history of contact dermatitis with benzoin compounds.

    When using this product avoid getting in the wound.

    Stop and ask a doctor if a rash develops.

    Flammable liquid Keep away from heat, sparks and open flame.

  • 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 and dry skin around the wound. • Gently squeeze vial to crush inner ampoule. • Allow tincture to saturate the tip of the vial, and carefully apply a thin film of the tincture to the skin on each side of the wound. • Allow tincture to dry (30 –40 seconds) before applying bandages.

  • Other Information

    Store at room temperature.

  • Inactive Ingredients

    Alcohol

  • Questions?

    Call 1-908-362-9266, Monday through Friday, 9:00am – 5:00pm e.s.t.

  • SPL UNCLASSIFIED SECTION

    DISPENSING SOLUTIONS®


    JAMES ALEXANDER CORPORATION
    Blairstown, NJ• (908) 362-9266
    Product information and MSDS available on-line at:
    www.james-alexander.com

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    BENZOIN 
    benzoin swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:46414-8888
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZOIN, (+/-)- (UNII: L7J6A1NE81) (BENZOIN, (+/-) - UNII:L7J6A1NE81) BENZOIN, (+/-)-0.6 g  in 0.6 mL
    ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9) ALOE.12 g  in 0.6 mL
    TOLU BALSAM (UNII: TD2LE91MBE) (BALSAM PERU - UNII:8P5F881OCY) TOLU BALSAM.24 g  in 0.6 mL
    LIQUIDAMBAR STYRACIFLUA RESIN (UNII: P41GWD11CX) (LIQUIDAMBAR STYRACIFLUA RESIN - UNII:P41GWD11CX) LIQUIDAMBAR STYRACIFLUA RESIN.48 g  in 0.6 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:46414-8888-260 mL in 1 BOX; Type 0: Not a Combination Product10/25/197602/28/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/25/197602/28/2025
    Labeler - James Alexander Corporation (040756421)
    Registrant - James Alexander Corporation (040756421)
    Establishment
    NameAddressID/FEIBusiness Operations
    James Alexander Corporation040756421manufacture(46414-8888)