Label: SIMPLIFY ANTIBACTERIAL HAND APPLE BLOSSOM SCENT- chloroxylenol soap

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

Drug Label Information

Updated December 12, 2023

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Chloroxylenol 0.30%

  • Purpose

    Antibacterial hand soap

  • Use

    For handwashing to decrease bacteria on the skin

  • Warnings

    For external use only

    KEEP OUT OF REACH OF CHILDREN.

    May cause moderate eye irritation. Avoid contact with eyes and skin. If in eyes, flush eyes gently with water for 15 minutes. If swallowed, drink water to dilute. If irritation persists, contact a Physician or Poison Control Center.

  • Directions

    • Wet hands.
    • Apply palmful to hands.
    • Scrub thoroughly and rinse with water.
  • Inactive Ingredients

    Carbamide, citric acid, cocamidopropyl betaine, DMDM hydroton, dodecylbenzene sulfonic acid, ethyl alcohol, fragrance, lauramine oxide, sodium chloride, sodium hydroxide, sodium lauryl ether sulfate, sodium xylene sulfonate, water

  • 19.4 FL OZ (1.21 PT) 573 mL

    Compare to

    Dawn ® Ultra Green Apple

    Simplify ®

    Antimicrobial

    Hand Soap & Ultra Dish

    Detergent

    • Contains no

    phosphates

    • Cuts Grease

    APPLE

    BLOSSOM

    SCENT

    19.4 FL OZ (1.21 PT) 573 mL

    FrontBack

  • INGREDIENTS AND APPEARANCE
    SIMPLIFY ANTIBACTERIAL HAND  APPLE BLOSSOM SCENT
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0281
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DODECYLBENZENESULFONIC ACID (UNII: 60NSK897G9)  
    WATER (UNII: 059QF0KO0R)  
    UREA (UNII: 8W8T17847W)  
    SODIUM C12-14 ALKETH-3 SULFATE (UNII: 5G80BO01PI)  
    ALCOHOL (UNII: 3K9958V90M)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11822-0281-1573 mL in 1 BOTTLE; Type 0: Not a Combination Product08/09/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/09/2023
    Labeler - Rite Aid Corporation (014578892)