Label: HARBOR MIST ALCO-FOAM HAND SANITIZER- alcohol liquid

  • NDC Code(s): 81792-003-01
  • Packager: Von Drehle Corporation
  • 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 April 30, 2021

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active Ingredient

    Ethyl Alcohol 62%v/v

  • Purpose

    Sanitizer

  • Uses:

    For hand sanitizing to decrease bacteria on the skin that can cause disease.

    Recommended for repeated uses.

  • Warnings:

    Flammable. Keep away from fire or flame.

    For external use only.

    When using this product avoid contact with eyes.

    In case of eye contact, flush eyes with water.

    Stop use and ask a doctor if irritation or redness develops, or condition persists for more than 72 hours.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions:

    Place enough product in your palm to thoroughly cover your hands.

    Rub hands together briskly until dry.

    Children under 6 yearsof age should be supervised when using this product.

  • Other Information:

    Store below 110 F (43 C).

    May discolor certain fabrics or surfaces.

  • Inactive Ingredients:

    Aqua, DEA-C8-C18 Perfluoroalkylethyl Phosphate

  • PRINCIPAL DISPLAY PANEL

    Harbor

    HARBOR MIST ALCO-FOAM

    HAND SANITIZER

    QUESTIONS?

    Call 800-438-3631 or visit us online at harbortowelandtissue.com.

    1

    PET

    NSF

    Nonfood Compounds

    Program Listed (E3)

    (Registration #164058)

    Item #H740AS

    1250 ml (42 fl. oz.)

    Made in the U.S.A.

    container label

  • INGREDIENTS AND APPEARANCE
    HARBOR MIST ALCO-FOAM HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81792-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81792-003-011250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/30/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333E04/30/2021
    Labeler - Von Drehle Corporation (071054415)
    Establishment
    NameAddressID/FEIBusiness Operations
    Woodbine Products Company004220323manufacture(81792-003)