Label: ASEPSO LEMON SCENTED ANTISEPTIC- chloroxylenol soap

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

Drug Label Information

Updated October 27, 2023

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  • Drug Facts

  • Active ingredients

    Chloroxylenol 0.25%

    Purpose

    Antiseptic

  • Use

    • For hand washing to decrease bacteria on the skin.
  • Warnings

    For external use only

    Do not use

    in the eyes

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Wet hands and forearms. Apply a palmful to hands and forearms. Scrub thoroughly for 30-60 seconds. Rinse and repeat.
  • Other information

    • Do not use on fabrics. Store away from heat and humidity
  • Inactive ingredients

    Sodium Palmitate, Sodium Palm Kernelate, Water, Fragrance, Glycerin, Palm Acid, Liquid Paraffin, Sodium Chloride, Palm Kernel Acid, Tetrasodium EDTA, Synthetic Iron Oxides Color, Tetrasodium (1-hydroxyethylidene) Bisphosphonate, FD&C Yellow No 5.

  • Package Labeling:

    Label4

  • INGREDIENTS AND APPEARANCE
    ASEPSO LEMON SCENTED ANTISEPTIC 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49698-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL2.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM PALMITATE (UNII: JQ43KP6296)  
    SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PALM ACID (UNII: B6G0Y5Z616)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PALM KERNEL ACID (UNII: 79P21R4317)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49698-010-011 in 1 CARTON09/12/2023
    180 g in 1 CASE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)09/12/2023
    Labeler - CODAA SWITZERLAND AG (483467697)
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