Label: TRANSCEND ALCO-FOAM HAND SANITIZER- alcohol liquid

  • NDC Code(s): 81792-001-01
  • Packager: Von Drehle Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 8, 2024

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  • 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 use.

  • 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 irritationor redness develops, or if 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 years of 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, Acrylates/Perfluorohexylethyl Methacrylate Copolymer (and) Perfluorohexylethyl Alcohol

  • PRINCIPAL DISPLAY PANEL

    TRANSCEND

    by Marcal

    ALCO-FOAM HAND SANITIZER

    Manufactured for Marcal Paper

    QUESTIONS

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

    1

    PET

    Item #T740AS

    1250 ml (42 fl. oz.)

    Made in the U.S.A.

    NSF

    Nonfood Compounds

    Program Listed (E3)

    (Registration #161161)

    container label

  • INGREDIENTS AND APPEARANCE
    TRANSCEND ALCO-FOAM HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81792-001
    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
    2-(PERFLUOROHEXYL)ETHANOL (UNII: G2R5YO5N3V)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/PERFLUOROHEXYLETHYL METHACRYLATE COPOLYMER (SALUS AF) (UNII: HLB263IJK9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81792-001-011250 mL in 1 BOTTLE; Type 0: Not a Combination Product02/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/01/2023
    Labeler - Von Drehle Corporation (071054415)
    Establishment
    NameAddressID/FEIBusiness Operations
    Woodbine Products Company004220323manufacture(81792-001)
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