Label: ANTIMICROBIAL HAND WASH LAVENDER- benzalkonium chloride soap

  • 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 August 16, 2020

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  • ACTIVE INGREDIENT

    BENZALKONIUM CHLORIDE (.13%)

  • PURPOSE

    ANTIMICROBIAL

  • USE

    • FOR HANDWASHING TO DECREASE 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.

    STOP USE AND ASK A DOCTOR IF IRRITATION OR REDNESS DEVELOPS.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DIRECTIONS

    • PUMP INTO HANDS, WET AS NEEDED
    • LATHER VIGOROUSLY FOR AT LEAST 15 SECONDS
    • WASH SKIN, RINSE THOROUGHLY AND DRY
  • INACTIVE INGREDIENTS

    PURIFIED WATER (AQUA), SODIUM LAURETH SULFATE, COCAMIDOPROPYL BETAINE, SODIUM CHLORIDE, ALOE BARBADENSIS (ALOE VERA) LEAF JUICE, COCOS NUCIDERA (COCONUT) OIL, ARGANIA SPINOSA (ARGAN) KERNEL OIL, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, BUTYROSPERMUM PARKII (SHEA) BUTTER, CUCUMIS SATIVUS (CUCUMBER) FRUIT EXTRACT, GLYCERIN, POLYQUATERNIUM-7, PEG-150 DISTEARATE, PHENOXYETHANOL, DEHYDROACETIC ACID, BENZYL ALCOHOL, FRAGRANCE (PARFUM)

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Nature Love_Antimicrobial Hand Wash_Lavender_16oz

  • INGREDIENTS AND APPEARANCE
    ANTIMICROBIAL HAND WASH  LAVENDER
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78902-108
    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)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    JOJOBA OIL (UNII: 724GKU717M)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    CUCUMBER (UNII: YY7C30VXJT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)  
    PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DEHYDROACETIC ACID (UNII: 2KAG279R6R)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78902-108-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product08/16/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A08/16/2020
    Labeler - Jocott Brands, Inc. (080399826)
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