WET WIPES (BENZALKONIUM CHLORIDE) SWAB [DELTA BRANDS, INC]

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WET WIPES (BENZALKONIUM CHLORIDE) SWAB [DELTA BRANDS, INC]
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NDC 20276-431-16, 20276-431-30, 20276-431-36, 20276-431-40
Set ID 0b4d3aca-7876-457e-85b2-a2ade1fd135f
Category HUMAN OTC DRUG LABEL
Packager Delta Brands, Inc
Generic Name
Product Class
Product Number
Application Number PART333A
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  • 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 TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-431
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:20276-431-3030 in 1 PACKAGE; Type 0: Not a Combination Product01/23/2007
    2NDC:20276-431-3636 in 1 PACKAGE; Type 0: Not a Combination Product01/23/2007
    3NDC:20276-431-4040 in 1 PACKAGE; Type 0: Not a Combination Product06/06/2016
    4NDC:20276-431-1616 in 1 PACKAGE; Type 0: Not a Combination Product06/06/2016
    5NDC:20276-431-8080 in 1 PACKAGE; Type 0: Not a Combination Product10/04/2019
    6NDC:20276-431-6060 in 1 PACKAGE; Type 0: Not a Combination Product04/27/2020
    7NDC:20276-431-5050 in 1 PACKAGE; Type 0: Not a Combination Product09/23/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/23/2007
    Labeler - Delta Brands, Inc (102672008)
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