Label: ALCOHOL PREP PAD-LARGE- isopropyl alcohol swab

  • NDC Code(s): 72727-0001-2
  • Packager: Global Biomedical Technologies, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated July 11, 2023

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  • ACTIVE INGREDIENT:

    70% isopropyl alcohol, saturated prep pads.

  • PURPOSE:

    Bandage releasing agent.

  • USE:

    To release bandage from the skin.

  • WARNINGS:

    For external use only: Flammable, keep away from Fire or flame.

    DO NOT USE with electrocautery procedures or in the eyes. If contact occurs, flush eyes with water.

    STOP USE if irritation and redness develops. If condition persists consult your health care practitioner.

    KEEP OUT OF REACH OF CHILDREN. If swallowed get medical help or contact a Poison Control Center right away.

  • DIRECTIONS:

    Wipe vigorously over bandage for several seconds (to release bandage from the skin) and then discard. Store at room temperature (59° - 86°F).

  • INACTIVE INGREDIENT:

    purified water.

  • Principal Display Panel – Carton Label

    Comfort
    Release®

    Global Biomedical
    Technology

    FOR
    SENSITIVE SKIN

    • Water resistant
    • Breathable
    • Long lasting
    • Painless & trauma-free release*

    DERMATOLOGIST
    RECOMMENDED

    *Apply rubbing alcohol with a cotton ball or an alcohol prep pad
    to the bandage for painless, trauma-free removal.

    10 Comfort Release® Bandages

    2” x 4" [5.1 cm x 10.2 cm]

    Includes 20 Alcohol Prep Pads for Removal

    Principal Display Panel – Carton Label
  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PAD-LARGE  
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72727-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72727-0001-220 in 1 BOX03/20/2019
    10.4 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/20/2019
    Labeler - Global Biomedical Technologies, LLC (080609342)
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