Label: WET WIPES cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated May 31, 2020

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  • Active Ingredient(s)

    Alcohol, Benzalkonium Chloride, C12-14-Alkyldimethyl(Ethylbenzyl) Ammonium Chlorides, Ethylhexylglycerin, Chlorphenesin

  • Purpose

    Antiseptic, disinfection and surface cleaning

  • Use

    TO disinfect and deodorize hard, nonporous surfaces.

  • Warnings

    Back of Package

  • Do not use

    Do not use or store near heat or open flame.

  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    back

  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
    • Do not use or store near open heat or flame.
  • Inactive ingredients

    glycerin, purified water, fragrance

  • PRINCIPAL DISPLAY PANEL

    Front of Package

    Package Label - Principal Display Panel

    80 wipes

    NDC 7663-101-45

  • INGREDIENTS AND APPEARANCE
    WET WIPES 
    wet wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76693-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM (UNII: 7N6JUD5X6Y) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM0.06 g  in 100 g
    PHENOXYETHANOL (UNII: HIE492ZZ3T) (PHENOXYETHANOL - UNII:HIE492ZZ3T) PHENOXYETHANOL0.3 g  in 100 g
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B) (DIDECYLDIMONIUM - UNII:Z7F472XQPA) DIDECYLDIMONIUM CHLORIDE0.4 g  in 100 g
    CHLORPHENESIN (UNII: I670DAL4SZ) (CHLORPHENESIN - UNII:I670DAL4SZ) CHLORPHENESIN0.1 g  in 100 g
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX) 0.1 g  in 100 g
    WATER (UNII: 059QF0KO0R) 48.97 g  in 100 g
    FRAGRANCE LAVENDER & CHIA F-153480 (UNII: SXS9CO2TZK) 0.02 g  in 100 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76693-101-4580 g in 1 PACKAGE; Type 5: Device Coated or Otherwise Combined with Biologic07/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/15/2020
    Labeler - Sourcery Ltd (800787645)
    Registrant - Sourcery Ltd (800787645)
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