Label: LUCKY SUPERSOFT WET WIPES- benzalkonium chloride cloth

  • NDC Code(s): 20276-434-18, 20276-434-35, 20276-434-40, 20276-434-42, view more
    20276-434-60
  • 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 0.10%

  • Purpose

    Antiseptic

  • Uses

    ■ decreases bacteria on the 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       ■ apply to hands

    2 years and over          ■ allow to dry without wiping

    children under 2 years 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, tocopherol acetate

  • Package Label

    Package Label

  • INGREDIENTS AND APPEARANCE
    LUCKY SUPERSOFT  WET WIPES
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-434
    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)  
    PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    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:20276-434-3535 in 1 CANISTER; Type 0: Not a Combination Product01/15/2015
    2NDC:20276-434-4040 in 1 CANISTER; Type 0: Not a Combination Product01/15/2015
    3NDC:20276-434-1818 in 1 BOX; Type 0: Not a Combination Product02/18/2015
    4NDC:20276-434-6060 in 1 CANISTER; Type 0: Not a Combination Product03/01/2016
    5NDC:20276-434-4242 in 1 CANISTER; Type 0: Not a Combination Product09/16/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A01/15/2015
    Labeler - Delta Brands, Inc (102672008)
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