Label: ETHYL ALCOHOL WET WIPES- alcohol cloth

  • 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 September 17, 2020

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol (70.00% V/V)

    Purpose

    Antiseptic

  • Uses

    • For hand-washing to decrease bacteria on skin
  • Warnings

    Flammable. Keep away from heat and flame.
    For External use only.

    Do not use

    in eyes. In case of contact, rinse thoroughly with water.

    Stop use & ask doctor

    if rash/redness or irritation appears/develops and persist for more than 72 hours.

    Keep out of reach from children

    except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

  • Directions

    • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation. 
    • Thoroughly wipe hands, allow to dry without washing.
    • Discard after single use
  • Other information

    • Do not flush down toilet. 
    • Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit) 
    • May discolor certain fabrics
  • Inactive Ingredients

    Aqua, Glycerin, Aloe Barbadensis Leaf Juice, D-Panthenol, Phenoxyethanol

  • Package Labeling:15pcs

    Bottle

  • Package Labeling:50pcs

    Bottle2

  • INGREDIENTS AND APPEARANCE
    ETHYL ALCOHOL WET WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73796-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73796-003-0215 in 1 PACKAGE08/20/2020
    13.6 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    2NDC:73796-003-0350 in 1 PACKAGE08/20/2020
    23.6 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E08/20/2020
    Labeler - ProStock LLC (078859574)
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