Label: LUCKY ANTIBACTERIAL- benzalkonium chloride liquid

  • NDC Code(s): 20276-147-09, 20276-147-11, 20276-147-12, 20276-147-14, view more
    20276-147-15, 20276-147-16, 20276-147-40, 20276-147-64, 20276-147-75
  • 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 January 14, 2021

If you are a consumer or patient please visit this version.

  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antibacterial

  • Uses

    for hand washing to decrease bacteria on the skin

  • Warnings

    For external use only

  • When using this product

    ■ avoid contact with the eyes. In case of eye contact, flush with water.

  • Stop use and ask a doctor if


    ■ irritation and redness develops

  • Keep out of reach of children

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

  • Directions

    ■ pump into hands, wet as needed ■ lather vigorously for at least 15 seconds ■ wash skin, rinse thoroughly and dry

  • Inactive ingredients

    water, cocamidopropyl betaine, cetrimonium chloride, coco-glucoside, glyceryl oleate, cocamide MEA, glycerin, PEG-150 distearate, sodium chloride, fragrance, citric acid, methylchloroisothiazolinone, methylisothiazolinone, FDC blue no. 1

  • Package Label

    package label

  • INGREDIENTS AND APPEARANCE
    LUCKY  ANTIBACTERIAL
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:20276-147
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    COCO MONOETHANOLAMIDE (UNII: C80684146D)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:20276-147-12400 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/10/2016
    2NDC:20276-147-75221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    3NDC:20276-147-09266 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    4NDC:20276-147-11333 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    5NDC:20276-147-14414 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    6NDC:20276-147-15444 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    7NDC:20276-147-16500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    8NDC:20276-147-401180 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    9NDC:20276-147-641890 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/10/2016
    Labeler - Delta Brands, Inc (102672008)