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Wet Wipes (Delta Brands, Inc)

Available Formats

Dosage Form Package Information Links
SWAB 30 SWAB in 1 PACKAGE (20276-431-30) Label Information
SWAB 36 SWAB in 1 PACKAGE (20276-431-36) Label Information

Complete Wet Wipes Information

  • Active Ingredient

    Benzalkonium Chloride 0.1%


  • Purpose

    Antiseptic


  • Uses

    decreases bacteria on the skin


  • Warnings

    For external use only


  • Do not use

    Over large areas of the body if you are allergic to any of the ingredients


  • When using this product


    do not get into eyes. If contact occurs, rinse thoroughly with water.


  • Stop use

    Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours


  • 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

      for adults and children 2 years and over use on hands and face to clean and refresh, allow skin to air dry.  For children under 2 years of age ask a doctor before use.


  • Inactive Ingredients

    water, propylene glycol, cocamidopropyl betaine, peg-7 glyceryl cocoate, fragrance, benzyl alcohol, methylchloroisothiazolinine, methylisothiazolinone, tetrasodium EDTA, peg-40 hydrogenated castor oil, cetrimonium chloride, citric acid, aloe vera extract, alphatocopherol acetate


  • Package Label

    Package Label


  • INGREDIENTS AND APPEARANCE
    WET WIPES 
    benzalkonium chloride swab
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:20276-431
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 0.1 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:20276-431-30 30 in 1 PACKAGE; Type 0: Not a Combination Product 01/23/2007
    2 NDC:20276-431-36 36 in 1 PACKAGE; Type 0: Not a Combination Product 01/23/2007
    3 NDC:20276-431-40 40 in 1 PACKAGE; Type 0: Not a Combination Product 06/06/2016
    4 NDC:20276-431-16 16 in 1 PACKAGE; Type 0: Not a Combination Product 06/06/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/23/2007
    Labeler - Delta Brands, Inc (102672008)