Label: PERSONAL CARE WET WIPES CITRUS- benzalkonium chloride cloth

  • NDC Code(s): 20276-436-01, 20276-436-15, 20276-436-18, 20276-436-30, view more
    20276-436-40
  • 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 December 16, 2022

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  • Active ingredient

    Benzalkonium chloride 0.13%

  • Purpose

    Antiseptic

  • Uses

    for hand sanitizing to decrease bacteria on skin

  • Warnings

    For external use only

  • Do not use

    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 and ask a doctor if

    irritation or rash develops and continues for more than 72 hours

  • Keep out of reach of children

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

  • Directions

    adults and children 2 years and over ■ apply to hands ■ allow to dry without wiping

    children under 2 years ask a doctor before use

  • Inactive ingredients

    water, ethyl alcohol, aloe barbadensis leaf juice, PEG-60 lanolin, fragrance, tetrasodium EDTA, phenoxyethanol, potassium sorbate, quaternium-52, citric acid

  • Package Label

    packet label

  • INGREDIENTS AND APPEARANCE
    PERSONAL CARE WET WIPES  CITRUS
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-436
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g
    Inactive Ingredients
    Ingredient NameStrength
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PEG-60 LANOLIN (UNII: K2OI1D27ET)  
    QUATERNIUM-52 (UNII: 588EQF3H1P)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:20276-436-1515 in 1 BOX01/07/2021
    1NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:20276-436-1818 in 1 BOX01/07/2021
    2NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:20276-436-3030 in 1 BOX01/07/2021
    3NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:20276-436-4040 in 1 BOX01/07/2021
    4NDC:20276-436-011 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/07/2021
    Labeler - Delta Brands, Inc (102672008)
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