Label: WET WIPES- benzalkonium chloride swab

  • NDC Code(s): 20276-431-16, 20276-431-30, 20276-431-36, 20276-431-40, view more
    20276-431-50, 20276-431-60, 20276-431-80
  • Packager: Delta Brands, Inc
  • 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 July 7, 2023

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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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