Label: CHEMSEPTIC- chloroxylenol soap

  • NDC Code(s): 59503-0544-1, 59503-0544-2, 59503-0544-3, 59503-0544-4, view more
    59503-0544-5, 59503-0544-6, 59503-0544-7, 59503-0544-8, 59503-0544-9
  • Packager: Rochester Midland Corporation
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 18, 2025

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  • Drug Facts Box OTC-Active Ingredient Section

    Chloroxylenol 0.3%

  • Drug Facts Box OTC-Purpose Section

    Antiseptic

  • Drug Facts Box OTC-Indications & Usage Section

    for hand-washing to decrease bacteria on the skin

  • Drug Facts Box OTC-Warnings Section

    For external use only

  • Drug Facts Box OTC-When Using Section

    do not get into eyes

    if contact occurs, rinse eyes thoroughly with water

  • Drug Facts Box OTC-Stop Use Section

    irritation and redness develop

  • Drug Facts Box OTC-Keep Out of Reach of Children Section

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

  • Drug Facts Box OTC-Dosage & Administration Section

    • wet hands and forearms
    • apply 5 milliliters (teaspoonful) or palmful to hands and forearms
    • scrub thoroughly for 1 minute and rinse
  • Drug Facts Box OTC-Inactive Ingredient Section

    water, decyl glucoside, sodium laureth sulfate, cocamide MIPA, propylene glycol, sodium chloride, citric acid, fragrance, FD and C yellow no.5, food red 10

  • Chemseptic 1 gallon

    product label

    Chemseptic  1 gallon label

  • INGREDIENTS AND APPEARANCE
    CHEMSEPTIC 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59503-0544
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59503-0544-1532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/200411/18/2025
    2NDC:59503-0544-23785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2004
    3NDC:59503-0544-318900 mL in 1 PAIL; Type 0: Not a Combination Product03/30/200411/18/2025
    4NDC:59503-0544-4208200 mL in 1 DRUM; Type 0: Not a Combination Product03/30/200411/18/2025
    5NDC:59503-0544-5946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/200411/18/2025
    6NDC:59503-0544-62500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2004
    7NDC:59503-0544-775600 mL in 1 DRUM; Type 0: Not a Combination Product03/30/200411/18/2025
    8NDC:59503-0544-8132500 mL in 1 DRUM; Type 0: Not a Combination Product03/30/2004
    9NDC:59503-0544-9650 mL in 1 BAG; Type 0: Not a Combination Product03/30/200411/18/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/30/2004
    Labeler - Rochester Midland Corporation (002207041)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABC Compounding Co., Inc.003284353manufacture(59503-0544)
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