Label: DIAL PROFESSIONAL FOAMING HAND SANITIZER liquid

  • 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 May 1, 2020

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  • DRUG FACTS

  • Active Ingredient(s)

    Ethyl Alcohol 65% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    Hand Sanitizer to help reduce bacteria that potentially can cause disease.

  • Warnings

    For external use only. Flammable. Keep away from fire or flame

  • WHEN USING

    When using this product avoid contact with face, eyes, and broken skin. if eye contact occurs, flush thoroughly with water and seek medical advice.

    Stop use and ask a doctor if irritation or redness develops.

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

  • KEEP OUT OF REACH OF CHILDREN

  • Directions

    • Put foam into DRY hands, wet hands thoroughly and rub into skin until dry.
    • Children under 6 years of age should be supervised by an adult when using this product.
  • Inactive ingredients


    Aqua (Water, Eau)· PEG-10 Dimethicone · Glycerin · Cocamidopropyl PG-Dimonium Chloride· lsopropyl Myristate ·
    PEG-12 Allyl Ether· T-Butyl Alcohol · Diazolidinyl Urea · Methylparaben

  • Questions

    1-877-777-3277

  • Legal Entity

    ®,TM,©2018 Distributed by
    Henkel Corporation,
    Rocky Hill, CT 06067
    www.dialprofessional.com

  • Package Label - Principal Display Panel

    Frontback450 mL NDC: 50663-004-01

  • INGREDIENTS AND APPEARANCE
    DIAL PROFESSIONAL FOAMING HAND SANITIZER 
    dial professional foaming hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50663-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62.75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
    COCAMIDOPROPYL PG-DIMONIUM CHLORIDE (UNII: 205Z54J075)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    GLYCERIN (UNII: PDC6A3C0OX) 0.857 mL  in 100 mL
    WATER (UNII: 059QF0KO0R) 33.97 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50663-004-01450 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/01/2020
    Labeler - Zotos International Inc (966706145)
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