Label: CLOROX ANTIBACTERIAL HAND - CHERRY AND MAGNOLIA BLOSSOM- chloroxylenol 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 January 5, 2016

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  • SPL UNCLASSIFIED SECTION

    DRUG FACTS

  • Active Ingredient

    Chloroxylenol (0.3%)

  • Purpose

    Antibacterial hand soap

  • Uses

    • Helps to decrease bacteria on the skin.
  • Warnings

    For external use only.

    Keep out of reach of children, except under adult supervision. In case of accidental ingestion, drink a glass of water to dilute. If eye contact occurs, rinse thoroughly with water.

  • Directions

    • Apply onto wet hands, lather for at least 30 seconds and rinse thoroughly.
  • Inactive Ingredients

    WATER (AQUA, EAU), SODIUM LAURETH SULFATE, PEG-4 RAPESEEDAMIDE,PANTHENOL,TOCOPHERYL ACETATE, BUTYROSPERMUM PARKII (SHEA) BUTTER EXTRACT, COCOS NUCIFERA (COCONUT) FRUIT EXTRACT, COCAMIDOPROPYL BETAINE, PEG-150 DISTEARATE, POLYSORBATE 20, GLYCERIN, ASCORBIC ACID, BIOTIN, NIACINAMIDE, PROPYLENE GLYCOL, SODIUM CHLORIDE, CITRIC ACID, PEG/PPG-18/18 DIMETHICONE, SODIUM HYDROXIDE, TETRASODIUM EDTA, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, FRAGRANCE (PARFUM), RED 40 (CI 16035), RED 33 (CI 17200), EXT. VIOLET 2 (CI 60730), LIMONENE, LINALOOL.

  • Questions?

    1-855-539-3564

  • SPL UNCLASSIFIED SECTION

    Distributed by Brand Buzz LLC,
    1400 Broadway, New York, NY 10018

  • PRINCIPAL DISPLAY PANEL - 295 mL Bottle Label

    CLOROX™

    antibacterial

    HAND SOAP
    DERMATOLOGIST TESTED

    MOISTURIZING

    cherry &
    magnolia blossom

    10 FL OZ (295 mL)

    PRINCIPAL DISPLAY PANEL - 295 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    CLOROX ANTIBACTERIAL HAND - CHERRY AND MAGNOLIA BLOSSOM 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69540-0076
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Chloroxylenol (UNII: 0F32U78V2Q) (Chloroxylenol - UNII:0F32U78V2Q) Chloroxylenol0.003 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Sodium Laureth-3 Sulfate (UNII: BPV390UAP0)  
    PEG-4 Rapeseedamide (UNII: 89575CN928)  
    Panthenol (UNII: WV9CM0O67Z)  
    .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
    Shea Butter (UNII: K49155WL9Y)  
    Coconut (UNII: 3RT3536DHY)  
    Cocamidopropyl betaine (UNII: 5OCF3O11KX)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    PEG-150 Distearate (UNII: 6F36Q0I0AC)  
    Polysorbate 20 (UNII: 7T1F30V5YH)  
    Glycerin (UNII: PDC6A3C0OX)  
    Ascorbic Acid (UNII: PQ6CK8PD0R)  
    Biotin (UNII: 6SO6U10H04)  
    Niacinamide (UNII: 25X51I8RD4)  
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    PEG/PPG-18/18 Dimethicone (UNII: 9H0AO7T794)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Edetate Sodium (UNII: MP1J8420LU)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
    Linalool, (+/-)- (UNII: D81QY6I88E)  
    Product Characteristics
    ColorREDScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69540-0076-1295.735 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart333E02/01/2015
    Labeler - Brand Buzz (079266204)
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