Label: EVERSOFT FOAMING HAND ANTI-BACTERIAL- chloroxylenol soap

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 September 29, 2022

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  • ACTIVE INGREDIENT

    Chloroxylenol @ 0.45%

  • PURPOSE

    ANTISEPTIC

  • USE

    Help prevent cross contaminatioo by hand contact to reduce inlcidence on nosocomial infection.

  • warnings

    For external use only. Avoid food contamination during application and storage.


    When using this product

    • Avoidcontact witheyes. ln case of contact wlth eyes, flush thoroughly with water
    • Avoid contact with broken skin.

    Stop use this product and ask a doctor if

    • Conditions worsen or irritation persists.
    • lrritation or redness develops and persisted for more than 72 hours
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children
    lf swallowed,get medical help or contact Poison Control Center right away.

  • directions

    • Wet Hands and forearms.
    • Apply a small amount of soap and scrub thoroughly for 1 minute.
    • Rinse thoroughly.
    • Dry hands completely.
  • OTHER INFORMATION

    • Store at 20-25°C (60 to 77°F)
  • INACTIVE INGREDIENTS

    Water, Sodium Laureth Sulfate, Propylene Glycol, Polyquatemium 7, Fragrance, Citric Acid, Color Dye.

  • PRINCIPAL DISPLAY PANEL

    01b LBL_Eversoft Foaming Hand Soap_1000mL

  • INGREDIENTS AND APPEARANCE
    EVERSOFT FOAMING HAND  ANTI-BACTERIAL
    chloroxylenol soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83019-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL0.45 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83019-101-111000 mL in 1 CONTAINER; Type 0: Not a Combination Product09/29/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/29/2022
    Labeler - Draco Hygienic Products Inc. (839066156)
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