Label: ALPET Q E2- benzalkonium chloride liquid

  • NDC Code(s): 59900-130-01, 59900-130-02, 59900-130-03, 59900-130-04
  • Packager: Best Sanitizers, 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 2, 2019

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  • Active Ingredient

    Benzalkonium Chloride 0.12%

  • Purpose

    Antiseptic Hand Cleanser

  • Uses

    • Hanwash to help reduce bacteria that potentially can cause diseases
    • Helps to prevent cross contamination by hand contact
    • Helps to prevent drying of the skin
    • Recommended for repeated use
  • Warnings

    • For external use only
  • When Using this product

    • Do not use in or near eyes
  • Keep out of reach of children

    In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

  • Directions

    • Wet hands and forearms
    • Apply an application to hands and forearms
    • Scrub thoroughly for at least 30 seconds (include the fingernails and the cuticles)
    • Rinse
  • Other information

    Store in a cool dry place below 104° F

  • Inactive ingredients

    water, glycerine, cocoamidopropy betaine, polyethylene-polypropylene glycol, benzyl alcohol, phenoxyethanol, tetra sodium EDTA, dehydroacetic acid

  • Questions?

    Contact Best Sanitizers Mon-Fri 9am-4pm PST at 888-225-3267

  • PRINCIPAL DISPLAY PANEL

    Alpet Q E2 Sanitizing Foam Soap

    NSF

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    ALPET Q E2 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59900-130
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.2 g  in 1000 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59900-130-011250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/2009
    2NDC:59900-130-023785.41 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/15/2009
    3NDC:59900-130-03208198 mL in 1 DRUM; Type 0: Not a Combination Product07/15/2009
    4NDC:59900-130-04946353 mL in 1 DRUM; Type 0: Not a Combination Product07/15/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E07/15/2009
    Labeler - Best Sanitizers, Inc (957473614)
    Establishment
    NameAddressID/FEIBusiness Operations
    Best Sanitizers, Inc627278224manufacture(59900-130)
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