Label: ISOPROPYL ALCOHOL cloth

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 6, 2024

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  • ACTIVE INGREDIENT

    70% Isopropyl Alcohol

  • INDICATIONS & USAGE

    Apply topically as needed. Single use only.

  • Intended Use

    For preparation of the skin prior to injection.

  • Warnings

    For external use only. Flammable, keep away from fire of flame. Do not use with electrocautery procedures or near eyes. Stop use and ask doctor if irritation or redness develop.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Wipe injection site vigorously and discard.

  • Inactive ingredients

    Purified water

  • SPL UNCLASSIFIED SECTION

    Distributed by Sarnova, HC, LLC's family of companies:
    Bound Tree Medical, LLC, Cardio Partners, Inc.
    Emergency Medical Products, Inc. &
    Tri-anim Health Services, Inc.
    5000 Tuttle Crossing Blvd.
    Dublin, OH 43016

  • PRINCIPAL DISPLAY PANEL - 0.4 mL Pouch Label

    curaplex®

    Alcohol Pad

    Large
    70% Isopropyl Alcohol

    For External Use Only

    Apply topically as needed. Single use only.

    Intended Use: For preparation of the
    skin prior to injection.

    Qty. 1

    STERILE R

    Sterility
    guaranteed
    unless package
    is opened or
    damage

    Do not reuse

    REF #1330-86100

    Not made with
    natural rubber latex

    Principal Display Panel - 0.4 mL Pouch Label
  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81085-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81085-0002-10.8 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)04/05/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH DRUGM00304/05/2022
    Labeler - Sarnova, Inc. (829320808)
    Registrant - ASP Global (080361159)
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