Label: PURIFI HAND SANITIZER- benzalkonium chloride solution

  • NDC Code(s): 80659-301-01, 80659-301-02, 80659-301-03, 80659-301-04, view more
    80659-301-05
  • Packager: Purifi LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 31, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium Chloride 0.13%

  • PURPOSE

    Purpose

    Antimicrobial

  • INDICATIONS & USAGE

    Uses

    Hand sanitizing to help reduce bacteria on the skin

  • WARNINGS

    Warnings

    For external use only.

    When using this productavoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

    ​Stop use and ask a doctor ifirritation or redness appears and lasts

    Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center immediately.

  • DOSAGE & ADMINISTRATION

    Directions

    Apply liberally to hands and gently rub until dry. Reapply every 6 hours.

  • STORAGE AND HANDLING

    Other information

    Store above 32°F (0°C) and below 100°F (38.8°C)

  • INACTIVE INGREDIENT

    Inactive ingredients

    purified water, glycerin, aloe barbadensis leaf juice

  • Product label

    image description

  • INGREDIENTS AND APPEARANCE
    PURIFI HAND SANITIZER 
    benzalkonium chloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80659-301
    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)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80659-301-01250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/10/2020
    2NDC:80659-301-0260 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/10/2020
    3NDC:80659-301-033800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/10/2020
    4NDC:80659-301-0450 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/10/2020
    5NDC:80659-301-05296 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/10/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00712/10/2020
    Labeler - Purifi LLC (117568842)
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