Label: PALM- chloroxylenol soap

  • NDC Code(s): 62257-544-06, 62257-544-07, 62257-544-10, 62257-544-11, view more
    62257-544-12, 62257-544-13, 62257-544-14, 62257-544-17, 62257-544-27, 62257-544-35, 62257-544-55
  • Packager: ABC Compounding Co., Inc.
  • Category: HUMAN OTC DRUG LABEL

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 December 26, 2018

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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, DMDM hydantoin, citric acid, fragrance, FD and C yellow no.5, food red 10

  • Palm 6544 Drug Facts and Label

    product label

    6544 Palm Label

  • INGREDIENTS AND APPEARANCE
    PALM  
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62257-544
    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:62257-544-17532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/21/1998
    2NDC:62257-544-07700 mL in 1 BAG; Type 0: Not a Combination Product12/21/1998
    3NDC:62257-544-101000 mL in 1 CARTRIDGE; Type 0: Not a Combination Product12/21/1998
    4NDC:62257-544-111000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/21/1998
    5NDC:62257-544-121000 mL in 1 BAG; Type 0: Not a Combination Product12/21/1998
    6NDC:62257-544-061 in 1 BOX12/21/1998
    6NDC:62257-544-13800 mL in 1 BAG; Type 0: Not a Combination Product
    7NDC:62257-544-143785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/21/1998
    8NDC:62257-544-27800 mL in 1 CARTRIDGE; Type 0: Not a Combination Product12/21/1998
    9NDC:62257-544-55208200 mL in 1 DRUM; Type 0: Not a Combination Product12/21/1998
    10NDC:62257-544-35132500 mL in 1 DRUM; Type 0: Not a Combination Product12/21/1998
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E12/21/1998
    Labeler - ABC Compounding Co., Inc. (003284353)
    Registrant - ABC Compounding Co., Inc. (003284353)
    Establishment
    NameAddressID/FEIBusiness Operations
    ABC Compounding Co., Inc.003284353manufacture(62257-544)
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