Label: ALCOHOL WIPES 75% ALCOHOL- honour hand sanitizing wipes 75% 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 December 17, 2021

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  • Main Ingredients

    75% alcohol

  • Purpose

    /

  • INDICATIONS & USAGE

    Open the lid and the sticker, pull out the wipes needed and then press the sticker back and close the lid to avoid alcohol evaporation.

  • WARNINGS

    Contains 75% ethanol alcohol. Keep away from heat and fire source. Place in dry and cool areas

  • DO NOT USE

    Do not use on sensitive position, like face eye, nose and mouth

  • WHEN USING

    1. Contains 75% ethanol alcohol. Keep away from heat and fire source. Place in dry and cool areas
    2. Keep away from Children
    3. Do not use on sensitive position, like face eye, nose and mouth
    4. Do not flush into toilet

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

    Keep away from Children

  • DOSAGE & ADMINISTRATION

    /

  • STORAGE AND HANDLING

    /

  • Inactive ingredients

    purified water (aqua), Aloe Leaf Extract, Glycerin, Benzalkonium chloride

  • Package Label - Principal Display Panel

    Label 300 wipes

    300 wipes NDC 78082-026-01

    Package 800 wipes

    Label 800 wipes

    800 wipes NDC 78082-026-02

    Package 150 wipes

    Label 150 wipes

    150 Wipes NDC 78082-026-03

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPES 75% ALCOHOL 
    honour hand sanitizing wipes 75% alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78082-026
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78082-026-01300 in 1 BAG; Type 0: Not a Combination Product05/18/2021
    2NDC:78082-026-02800 in 1 BAG; Type 0: Not a Combination Product05/18/2021
    3NDC:78082-026-03150 in 1 BAG; Type 0: Not a Combination Product05/18/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/18/2021
    Labeler - PICO INC. (203063060)
    Establishment
    NameAddressID/FEIBusiness Operations
    American Hygienics Corporation545198454manufacture(78082-026)
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