Label: CURAPLEX ALCOHOL PREP PAD- isopropyl alcohol swab

  • NDC Code(s): 81085-0001-1, 81085-0001-2
  • Packager: Sarnova, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 12, 2024

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

  • Active ingredient:

    Isopropyl Alcohol 70%

  • Purpose:

    Antiseptic Cleanser

  • Use

    For preparation of the skin prior to an injection.

  • Warnings:

    For external use only.

    Do not use:

    • with electrocautery procedures ν
    • in the eyes. If contact occurs, flush eyes with water.

    Flammable, keep away from fire or flame.

    Stop use and ask a doctor if irritation and 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.

  • Other Information

    Store at room temperature.

  • Inactive ingredients

    purified water

  • Questions?

    855-287-2759

  • Principal Display Panel - 0.4 mL Pouch Box Case Label

    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
    855.287.2759
    www.curaplex.com

    curaplex®

    Alcohol Pad

    Medium
    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. 20

    REF #1330-85300
    YYYY-MM-DD
    LOT
    XMMDDFC

    NDC 81085-0001-1

    Warnings: For external use only. Flammable, keep
    away from fire of flame. Do not use with electrocau-
    tery 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.

    STERILE R

    Sterility guaranteed unless package is
    opened or damage

    Do not reuse

    Not made with natural rubber latex

    Made in China

    Principal Display Panel - 0.4 mL Pouch Box Case Label
  • Principal Display Panel - 0.8 mL Pouch Box Case Label

    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
    855.287.2759
    www.curaplex.com

    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. 10

    REF #1330-86100
    YYYY-MM-DD
    LOT
    XMMDDFC

    NDC 81085-0001-2

    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.

    STERILE R

    Sterility guaranteed unless package
    is opened or damage

    Do not reuse

    Not made with natural rubber latex

    Made in China

    Principal Display Panel - 0.8 mL Pouch Box Case Label
  • INGREDIENTS AND APPEARANCE
    CURAPLEX ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81085-0001
    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:81085-0001-120 in 1 CASE09/13/2017
    1200 in 1 BOX
    10.4 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    2NDC:81085-0001-210 in 1 CASE09/13/2017
    2100 in 1 BOX
    20.8 mL in 1 POUCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH DRUGM00309/13/2017
    Labeler - Sarnova, Inc. (829320808)
    Registrant - ASP Global (080361159)