Label: WIPESPLUS HAND SANITIZING WIPES- ethyl alcohol cloth

  • Category: HUMAN OTC DRUG LABEL

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 October 14, 2022

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  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • For hand sanitizing to decrease bacteria on the skin.
    • Apply topically to the skin to help prevent cross contamination
    • Not recommended for repeated use.
    • Dries in seconds.
  • Warnings

    For external use only.

  • Flammable, keep away from fire or flame.

    Flammable, keep away from fire or flame.

  • Do not use

    • in or near the eyes
    • on open skin wounds or burns.
  • Stop use and ask a doctor

    • if irritation and redness develop
    • condition persists for more than 72 hours.
  • Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Remove lid.
    • Pull wipe from center of roll and thread theough opening in lid. Do not push finger through opening.
    • Replace lid, pull wipe up, and then at 45° angle. The next wipe dispenses automatically.
    • Close lid to retain moisture.
  • Other Information

    • Store at room temperature.
    • Dispose of used wipe in trash, do not flush into toilet.
  • Inactive Ingredients

    Aloe Barbadensis Extract, Benzalkonium Chloride, Citric Acid, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Water

  • Principal Display Panel

    wipesplus

    HAND SANITIZING WIPES

    • Killes 99.9% of germs

    240 CT

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  • INGREDIENTS AND APPEARANCE
    WIPESPLUS HAND SANITIZING WIPES 
    ethyl alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67151-737
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67151-737-01240 in 1 PACKAGE; Type 0: Not a Combination Product07/13/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/13/2022
    Labeler - Progressive Products, LLC (127111792)
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