Label: DISINFECTING WET WIPES patch

  • 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 April 24, 2021

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  • Active Ingredient(s)

    Ethyl Alcohol(75%)
    Benzalkonium Chloride(0.08%)

  • Purpose

    Disinfection
    Bacteriostat

  • Use

    ■Cleansing
    ■Disinfection
    ■Nursing

  • Warnings

    Ask a doctor before use if you have
    Patients with allergic skin Ask a doctor or pharmacist before use if you are
    When using this product
    Cleansing things
    Disinfecting things
    Travel period
    Keep out of reach of the children.
    Keep away from fire.

  • Do not use

    /

  • WHEN USING

    When using this product
    Cleansing things
    Disinfecting things
    Travel period
    Keep out of reach of the children.
    Keep away from fire.

  • STOP USE

    /

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the children.

  • Directions

    Tear Vnotch located on top of the plastic bag.
    Place entire bag inside of center pull dispenser.
    Close the lid of the dispenser.
    Pullout the first wipes approximately 6 to 8 inches from the center of the roll.
    Thread the wipe through the opening on the dispenser.
    Wipedispensingtensionmaybe adjusted on the top of the dispenser.
    Dispensermustbemountedwith wipes dispensing up.

  • Other information

    store below 35℃(95℉)

  • Inactive ingredients

    Cetylpyridinium Chloride, Didecyldimonium Chloride,
    Glycerin, Aloe Barbadensis Leaf Extract,
    Decylglucoside, Chamomilla Recutita Flower Extract, Aque

  • Package Label - Principal Display Panel

    81838-001-01 50CLOTH in 1BAG

    81838-001-01 50CLOTH in 1BAG

  • INGREDIENTS AND APPEARANCE
    DISINFECTING WET WIPES 
    disinfecting wet wipes patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81838-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 g  in 100 
    BENZALKONIUM (UNII: 7N6JUD5X6Y) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM0.08 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    WATER (UNII: 059QF0KO0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    CHRYSANTHEMUM X MORIFOLIUM WHOLE (UNII: BEI52721UI)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81838-001-0150 in 1 BAG; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/30/2020
    Labeler - Changzhou MeiMuSen New Material Technology Co., Ltd (715382258)
    Establishment
    NameAddressID/FEIBusiness Operations
    Changzhou MeiMuSen New Material Technology Co., Ltd715382258manufacture(81838-001)
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