Label: ZEP BLUE SKY AB- benzalkonium chloride liquid

  • NDC Code(s): 66949-124-11, 66949-124-24
  • Packager: Zep Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 18, 2024

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  • Active Ingredient

    Benzalkonium Chloride 0.13%

  • Purpose

    Antiseptic Handwash

  • Uses

    Hand washing to decrease bacteria on skin.

  • Warnings

    For external use only.

  • Do not use

    Do not use in or around the eyes ; if in eyes, rinse promptly and thoroughly with water.

  • When using this product

    • Do not swallow.
    • If swallowed, give large quantities of water to drink and consult a physician immediately.
  • Stop use and ask a doctor

    Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

  • Keep out of reach of children

    Keep out of reach of children except under adult supervision.

  • Directions

    • Wet hands with water.
    • Place hands under dispenser.
    • Apply foamed soap.
    • Massage soap into hands and wrists, emphasizing back of hands, knuckles, and cuticles.
    • Rinse hands thoroughly and dry.
  • Other information

    • Store at 20 to 25°C (68 to 77°F).
    • Do not freeze.
    • Dispose in accordance with all applicable federal, state and local regulations.
  • Inactive ingredients

    Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Di-PPG-2 Myreth-10 Adipate, Phenoxyethanol, Iodopropynyl Butylcarbamate, Methylisothiazolinone, Hexanediol, Tetrasodium Iminodisuccinate, Fragrance, Methylchloroisothiazolinone, Citric Acid, Blue 1

  • Questions or comments?

    Call 1-877-I-BUY-ZEP (1-877-428-9937)

  • PRINCIPAL DISPLAY PANEL

    124_3321

  • INGREDIENTS AND APPEARANCE
    ZEP BLUE SKY AB 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66949-124
    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)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDE (UNII: HY9O6ZW9CY)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DI-PPG-2 MYRETH-10 ADIPATE (UNII: 4IN301M0KJ)  
    HEXANEDIOL (UNII: ZIA319275I)  
    TETRASODIUM IMINODISUCCINATE (UNII: GYS41J2635)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66949-124-116000 mL in 1 CASE; Type 0: Not a Combination Product01/23/201712/31/2025
    2NDC:66949-124-2415140 mL in 1 CASE; Type 0: Not a Combination Product01/23/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/23/2017
    Labeler - Zep Inc. (030471374)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zep Inc.112125310manufacture(66949-124)
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