Label: PACIFIC BLUE ULTRA ANTIMICROBIAL PACIFIC CITRUS- benzalkonium chloride soap

  • NDC Code(s): 54622-712-01
  • Packager: Georgia-Pacific Consumer Products LP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 15, 2024

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  • Active ingredient

    Benzalkonium chloride 0.13% w/w

  • Purpose

    Antiseptic

  • Uses

    Handwash to help reduce bacteria that potentially can cause disease.

  • Warnings

    For external use only

  • When using this product

    Avoid contact with eyes.  In case of eye contact, flush with water.

  • Stop use and ask a doctor

    if irritation or redness develops.  If condition persists for more than 72 hours consult a doctor.

  • Keep out of reach of children.

    If swallowed, seek immediate medical attention or call a poison control center.

  • Directions

    Wet hands, apply soap, rub hand together vigorously for at least 20 seconds. Rinse and dry hand thoroughly with a disposable paper towel.

  • Inactive ingredients

    Water (Aqua), Lauramine Oxide, Lauryl Betaine, Lautrimonium Chloride, Glycerin, Sodium PCA, Tocopheryl Acetate, Oleth-10, Tetrasodium EDTA, Citric Acid, Fragrance, Yellow 6, Red 40

  • Adverse reaction

    Pacific Blue Ultra ™

    Antimicrobial Foam Soap

    Pacific Citrus ® - SKU 43819

    Manufactured for Georgia-Pacific Consumer Products. Atlanta, GA 30303

    Quesitons? Call 1-866-HELLOGP (435-5647)

    or visit us online at www.gppro.com

    (c) 2024 GP PRO. All rights reserved.

  • Principal display panel

    Antimicrobial Foam Soap

    1200 mL (40.5 FL OZ)

    mm01

  • INGREDIENTS AND APPEARANCE
    PACIFIC BLUE ULTRA ANTIMICROBIAL  PACIFIC CITRUS
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54622-712
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    OLETH-10 (UNII: JD797EF70J)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    LAURYL BETAINE (UNII: Y4P927Q133)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54622-712-011200 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/25/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)05/25/2016
    Labeler - Georgia-Pacific Consumer Products LP (806142217)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091520manufacture(54622-712)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(54622-712)
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