Label: ETHYL ALCOHOL- hand sanitizing wipes cloth

  • NDC Code(s): 67151-738-01
  • Packager: Progressive Products, 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 March 13, 2023

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  • Active Ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • Hand sanitizing wipes to help reduce bacteria on the skin.
  • Warnings

    For External use only.

    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 or redness develops
    • condition persists or get worse

    Keep out of reach of children

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

  • Directions

    • Pull back canster lid
    • Remove wipe
    • Close canister lid
    • Keep lid closed to retain moisture
    • Wet hands thoroughly with product and allow to dry without wiping
    • For single use only. Discard individual wipe after use
  • Other information

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

    Water, Propylene Glycol, Glycerin, Fragrance, Benzalkonium chloride, Tocopherol Acetate, Citric Acid, Aloe Barbadensis Leaf Juice

  • Principal Display Panel

    WAXIE

    Hand Sanitizing Wipes

    70% Alcohol Based

    Kills 99.9% of germs

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    12/240 CT CANISTERS

  • INGREDIENTS AND APPEARANCE
    ETHYL ALCOHOL 
    hand sanitizing wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67151-738
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67151-738-01240 in 1 BOX03/13/2023
    11 mL in 1 PACKAGE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/13/2023
    Labeler - Progressive Products, LLC (127111792)
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