Label: ILI HAND SANITIZER INSTANT- alcohol gel

  • 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 June 30, 2010

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  • ACTIVE INGREDIENT

    Active Ingredient: Ethyl Alcohol 63%

  • PURPOSE

    Purpose: Antiseptic

  • INDICATIONS & USAGE

    Use: For hand washing to decrease bacteria on the skin. Recommended for repeated use.

  • WARNINGS

    Warnings: Flammable, keep away from fire or flame. For external use only. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.

  • STOP USE

    Stop use and ask a doctor if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    Directions: Wet hands thoroughly with product and allow to dry without wiping.

  • QUESTIONS

    Questions? 1-323-284-9021 weekdays, 9am to 5pm PST

  • ili Hand Sanitizer 8 fl oz

    8 fl oz Ili Hand Sanitizer LabelMM1:8floz_ILI_Hand_Sanitizer_Label rev 3_Page_1.jpg

  • INACTIVE INGREDIENT

    water, isopropyl alcohol, glycerin, methyl gluceth-20, panthenol, tocopheryl acetate, benzalkonium chloride, polysorbate 20, carbomer, sodium benzotriazolyl butylphenol sulfonate, aminomethyl propanol, fragrance

  • INGREDIENTS AND APPEARANCE
    ILI HAND SANITIZER  INSTANT
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50859-100
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol63 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50859-100-01236.6 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E06/01/2010
    Labeler - Strong Brands, Inc. (962050543)
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