Label: AGROBAC PURE FOAM- benzalkonium chloride solution

  • NDC Code(s): 11084-024-01, 11084-024-12, 11084-024-20, 11084-024-27, view more
    11084-024-66
  • Packager: SC Johnson Professional USA, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 February 23, 2023

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  • Active ingredient

    Benzalkonium Chloride, 0.13%

  • Purpose

    Antibacterial

  • Uses

    for hand washing to reduce bacteria on the skin

  • Warnings

    For external use only

    When using this product

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

    Keep out of reach of children.

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

  • Directions

    apply to dry hands

    add water

    lather hands for 30 seconds

    rinse and dry hands thoroughly

  • Inactive ingredients

    Aqua (Water), Hexylene Glycol, Coco-Glucoside, Cocamidopropyl PG-Dimonium Chloride Phosphate, Laurtrimonium Chloride, PEG-6 Cocamide, Citric Acid

  • PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

    SCJ PROFESSIONAL
    A Family Company™

    NDC 11084-024-27

    AgroBac™ PURE

    ANTIMICROBIAL FOAM SOAP
    Dye & Fragrance-Free E2 Antibacterial Foam Handwash.

    NSF®
    Nonfood Compounds
    Program Listed E2
    157532

    1 L (33.8 fl oz)

    SC Johnson Professional USA, Inc.
    Charlotte, NC 28217
    1-800-248-7190. www.scjp.com

    Pat.www.scjp.com/patents

    deb
    SKIN CARE

    1000002834/0320

    PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
  • INGREDIENTS AND APPEARANCE
    AGROBAC PURE FOAM 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-024
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    COCO GLUCOSIDE (UNII: ICS790225B)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    PEG-6 COCAMIDE (UNII: YZ6NLA4O1E)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11084-024-271000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2018
    2NDC:11084-024-202000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2018
    3NDC:11084-024-121200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2018
    4NDC:11084-024-0147 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/201807/19/2021
    5NDC:11084-024-661000 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/01/2018
    Labeler - SC Johnson Professional USA, Inc. (607378015)
    Establishment
    NameAddressID/FEIBusiness Operations
    APEX International, Inc.015226132manufacture(11084-024)
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