Label: CASEYSLAVENDER- caseys hand soap lavender scent liquid

  • 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 June 14, 2023

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  • Active Ingredient(s)

    Benzalkonium Chloride (CAS NO: 68424-85-1), 0.13% .

    Purpose

    Antimicrobial

  • Use

    Helps eliminate bacteria on hands

  • WARNINGS

    For external use only.

    Do not use

    If you are allergic to any of the ingredients.

    Stop use and ask a doctor

    if irritation or rash occurs.

    Do not use in or near the eyes.

    In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.

    Keep out of reach of children.

    If swallowed, get medical help or contact a poison control center immediately.

  • Directions

    Wash hands and rinse

  • Inactive ingredients

    Water, Anhydrous Citric Acid, Cocamidopropylamine Oxide, Edetate Sodium, Fragrance, Glycerin, Lauramine Oxide, Magnesium Chloride, Magnesium Nitrate, Methylchloroisothiazolinone, Methylisothiazolinone, PEG-120 Methyl Glucose Dioleate, PEG-4 Rapeseedamide, Styrene/acrylamide Copolymer (mw 500000), Colorant CI 60725, Lavandula Angustifola Extract.

  • PURPOSE

    Antibacterial

  • PRODUCT LABELS

    Caseys1

  • INGREDIENTS AND APPEARANCE
    CASEYSLAVENDER 
    caseys hand soap lavender scent liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76557-051
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LAVANDULA ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    WATER (UNII: 059QF0KO0R)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76557-051-01500 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product06/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/01/2023
    Labeler - KYNC Design LLC (039933298)
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