Label: ALCOHOL WET WIPES- alcohol cloth

  • NDC Code(s): 74979-006-01, 74979-006-02, 74979-006-03
  • Packager: Robert Gordon Ind. Ltd.
  • 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 27, 2023

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 75% (v/v)

    purpose

    Antiseptic

  • Uses

    • For hand sanitizing to decrease bacteria on the 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

    When Using this product

    • avoid contact with eyes and mouth. If in ayes, flush thoroughly with water.
    • Discontinue use and contact a doctor if irritation and redness develop and conditions persis for more than 72 hours.

    Keep out of reach of children

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

  • Directions

    • Tear open packet and remove wipe.
    • Wet hands thoroughly with product and let hands air dry.
    • Throw used wipe in trash. Do not flush.
  • Inactive ingredient

    Water

  • Other Information

    • Store between 15-30 oC (59-86 oF)
    • Avoid freezing and excessive heat above 40 oC (104 oF)
  • Package Labeling:10count

    Alcohol 10x label

  • Package Labeling:40count

    Bottle6

  • Package Labeling:80count

    Bottle7

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WET WIPES 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74979-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.75 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74979-006-0110 in 1 PACKAGE08/20/2020
    14.5 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    2NDC:74979-006-0240 in 1 PACKAGE08/20/202004/15/2023
    24.75 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    3NDC:74979-006-0380 in 1 PACKAGE08/20/202004/15/2023
    34.75 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 - Robert Gordon Ind. Ltd. (070064709)
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