Label: COCONUT FOAMING HAND SANITIZER WITH NATURAL VITAMIN E AND ALMOND OIL- benzalkonium chloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 26, 2023

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  • DRUG FACTS

  • ACTIVE INGREDIENT

    Benzalkonium Chloride 0.12%

    PURPOSE

    Antimicrobial

  • USES

    • For hand sanitizing to decrease bacteria on the skin
    • Recommended for repeated use
  • WARNINGS

    For external use only. Avoid contact with eyes. In case of eye contact, flush with water. Discontinue use if irritation or redness occurs.

    Keep out of reach of children

    2 years of age and younger. If swallowed, get help or contact a Poison Control Center right away.

  • DIRECTIONS

    Apply to dry hands, rub together, & let dry.

  • INACTIVE INGREDIENTS

    Purified water, surfactant, vitamin E(natural, d-alpha tocopherol), almond oil (natural), polysorbate 20, isopropyl alcohol USP, natural essential oil complex, natutal coconut scent.

  • Package Labeling:

    label

  • INGREDIENTS AND APPEARANCE
    COCONUT FOAMING HAND SANITIZER WITH NATURAL VITAMIN E AND ALMOND OIL 
    benzalkonium chloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57660-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.2 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
    ACETAMIDOETHOXYETHANOL (UNII: LVX2APC4XR)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57660-004-0150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product03/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/01/2022
    Labeler - TJA Health LLC (078799634)
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