Label: DEVOLVER DISINFECTING WIPES (alkyl- c12-18 benzyl dimethyl ammonium chloride liquid

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

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Drug Label Information

Updated November 5, 2020

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  • ACTIVE INGREDIENTS

    Alkyl (C=12-18) benzyl dimethyl ammonium chloride 0.36%

  • PURPOSE

    Antiseptic

  • INACTIVE INGREDIENT

    2-phenoxyethanol, Glycerine, Alkyl(C=12-18) benzyl dimethyl ammonium chloride, Quaternary ammonium compounds, C12-18-alkyl[(ethylphenyl)methyl]dimethyl, chlorides, sodium benzoate, Cetylpyridinium chloride, lemon fragrance, Tocopheryl Acetate

  • DIRECTIONS for Use :

    1. Before first use : Remove cap and seal. Take the corner of the center sheet and thread it through the dispensing flap of the container cap. Replace cap.

    2. Open container and tear off sheet.

    3. Erase all dry-erase markings from surface to be cleaned.

    4. Wipe surface thoroughly and discard towelette.

    5. Keep the container cap closed after each use.

  • DIRECTIONS for Use :

    * Cleans and restores dry-erase surfaces

    * Use Dry-Erase Board Cleaning Wipes to remove dry-erase marker shadows, ghosting and stains

    * Safe, Low Odor, Non-Toxic and Flame Resistant

    * Hands stay clean

    * Safe to use on most surfaces

  • Warning :

    Wipes are safe for most surfaces, but always test in an inconspicuous area prior to use on entire surface.

  • CAUTION

    Do not use of cleaning skin, for personal cleansing or as a diaper wipe. Causes moderate eyes irritation. Avoid contact with eyes or clothing. Wash thoroughly with soap and water after handling.

  • CAUTION

    Stop use and ask a doctor if irritation or rash occurs.

    These may be signs of a serious condition.

  • CAUTION

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • FIRST AID : IF IN EYES :

    Hold eye open and rinse slowly and gently with water for 15-20 minutes.

    Remove contact lenses, If present, after the first 5 minutes, then continue rinsing eye.

    Call a poison control center for treatment advice.

    Have the product container or label with you when calling a poision control center or doctor, or going for treatment.

  • PHYSICAL OR CHEMICAL HAZARDS :

    Do not use or store near heat or open flame.

  • STORAGE AND DISPOSAL :

    Dispose of wipe in the trash after use.

    Do not flush.

    Tightly close lid between uses to retain moisture.

    Nonrefillable

  • PACKAGE LABEL

    500g NDC: 75001-205-01 Label

    300g NDC: 75001-206-02 Label

    400g NDC: 75001-206-03 Label

    600g NDC: 75001-206-04 Label

    800g NDC: 75001-206-05 Label

  • INGREDIENTS AND APPEARANCE
    DEVOLVER DISINFECTING WIPES 
    alkyl (c12-18) benzyl dimethyl ammonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75001-206
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS) (N-ALKYL DIMETHYL BENZYL AMMONIUM ION (C12-C18) - UNII:3QBE2Z8KR2) N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18)0.36 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    N-DIALKYL METHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 00MFZ4H95Z)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    FRAGRANCE LEMON ORC2001060 (UNII: K1725A7G95)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75001-206-01500 g in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
    2NDC:75001-206-02300 g in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
    3NDC:75001-206-03400 g in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
    4NDC:75001-206-04600 g in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
    5NDC:75001-206-05800 g in 1 BOTTLE; Type 0: Not a Combination Product10/08/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/08/2020
    Labeler - Devolver Cosmetics Co., Ltd (695733244)
    Registrant - Devolver Cosmetics Co., Ltd (695733244)
    Establishment
    NameAddressID/FEIBusiness Operations
    Devolver Cosmetics Co., Ltd695733244manufacture(75001-206)
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