Label: ETHYL ALCOHOL- wipes plus swab

  • 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 October 14, 2022

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  • Active ingredients

    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.

    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

    • Pull back reseal label.
    • Remover wipe.
    • Reseal label
    • Keep label closed to retain moisture.
  • 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, Tocopheryl Acetate, Citric Acid, Aloe Barbadensis Extract.

  • Principal Display Panel

    Wipesplus

    SANITIZING WIPES

    80CT

    PRE-MOISTENED TOWELETTES

    WIPES PLUS

  • INGREDIENTS AND APPEARANCE
    ETHYL ALCOHOL 
    wipes plus swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67151-707
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67151-707-0180 in 1 POUCH; Type 0: Not a Combination Product02/16/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/16/2022
    Labeler - PROGRESSIVE PRODUCTS, LLC (127111792)
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