Label: HAND GUARD HIGH FOAMING ANTISEPTIC HAND AND BODY WASH- chloroxylenol soap

  • NDC Code(s): 31507-876-01, 31507-876-03, 31507-876-05, 31507-876-06, view more
    31507-876-07, 31507-876-08, 31507-876-09, 31507-876-10, 31507-876-11, 31507-876-12, 31507-876-13, 31507-876-14, 31507-876-15, 31507-876-16, 31507-876-17, 31507-876-18, 31507-876-19, 31507-876-20, 31507-876-24, 31507-876-27, 31507-876-28, 31507-876-35, 31507-876-55
  • Packager: Wechem, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

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, DMDM hydantoin, fragrance, methylchloroisothiazolinone, methylisothiazolinone, aloe barbadensis, acid red 1

  • Hand Guard High Foaming Antiseptic Hand & Body Wash 6876

    product label

    Hand Guard High Foaming Hand and Body Wash

  • INGREDIENTS AND APPEARANCE
    HAND GUARD HIGH FOAMING ANTISEPTIC HAND AND BODY WASH 
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:31507-876
    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)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    ACID RED 1 (UNII: 3365R6427R)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:31507-876-061 in 1 BOX01/04/201711/18/2025
    1800 mL in 1 BAG; Type 0: Not a Combination Product
    2NDC:31507-876-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    3NDC:31507-876-24118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    4NDC:31507-876-011200 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/201711/18/2025
    5NDC:31507-876-03350 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/201711/18/2025
    6NDC:31507-876-05540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    7NDC:31507-876-07700 mL in 1 BAG; Type 0: Not a Combination Product01/04/201711/18/2025
    8NDC:31507-876-092000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/201711/18/2025
    9NDC:31507-876-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/201711/18/2025
    10NDC:31507-876-111000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    11NDC:31507-876-121000 mL in 1 BAG; Type 0: Not a Combination Product01/04/2017
    12NDC:31507-876-13800 mL in 1 BAG; Type 0: Not a Combination Product01/04/201711/18/2025
    13NDC:31507-876-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    14NDC:31507-876-15946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    15NDC:31507-876-28149 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    16NDC:31507-876-27800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product01/04/201711/18/2025
    17NDC:31507-876-55208200 mL in 1 DRUM; Type 0: Not a Combination Product01/04/201711/18/2025
    18NDC:31507-876-081 in 1 BOX01/04/201711/18/2025
    181000 mL in 1 BAG; Type 0: Not a Combination Product
    19NDC:31507-876-16236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    20NDC:31507-876-1850 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/04/201711/18/2025
    21NDC:31507-876-1918900 mL in 1 CONTAINER; Type 0: Not a Combination Product01/04/201711/18/2025
    22NDC:31507-876-2075600 mL in 1 DRUM; Type 0: Not a Combination Product01/04/201711/18/2025
    23NDC:31507-876-35132500 mL in 1 DRUM; Type 0: Not a Combination Product01/04/201711/18/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/04/2017
    Labeler - Wechem, Inc. (010397446)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABC Compounding Co., Inc.003284353manufacture(31507-876)
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