Label: DUKAL ALCOHOL PREP PAD- isopropyl alcohol swab

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 3, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active Ingredients

    Isopropyl Alcohol 70%

  • PURPOSE

    Purpose

    Antiseptic Cleanser

  • INDICATIONS & USAGE

    Apply topically as needed to cleanse

  • WARNINGS

    Warnings

    • For External Use Only
    • Flammable, Keep away from fire or flame
  • DO NOT USE

    Do Not Use

    • with electrocautery procedures
    • In the Eyes. If contact occurs, flush eyes with water
  • STOP USE

    Stop Use

    If irritation and redness develop. If condition persists, consult your health care practitioner.

  • 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.

  • DOSAGE & ADMINISTRATION

    Directions

    Wipe injection site vigorously and discard.

  • STORAGE AND HANDLING

    Other Information

    Store at Room Temperature 15 - 30 C (59 - 86 F)


  • INACTIVE INGREDIENT

    Inactive Ingredient

    purified water

  • PRINCIPAL DISPLAY PANEL

    Dukal

    Alcohol Pad

    Non-Sterile

    Saturated with 70% Isopropyl Alcohol

    For External Use Only

    Not made with natural rubber latex / Single Use

    Manufactured For: Dukal, LLC

    1(800)243-0741 /Ronkonkoma, NY 11779 / dukal.com

    Made in China

    Dukal is a trademark registered in the

    US Patent & Trademark Office by Dukal, LLC

    1 Per Pouch / NDC 65517-0001-1 / REF 852

    852

  • INGREDIENTS AND APPEARANCE
    DUKAL ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65517-0001-10.4 mL in 1 POUCH; Type 0: Not a Combination Product05/01/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/01/2010
    Labeler - Dukal LLC (791014871)
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