Label: TRANSCEND E2 SANITIZING FOAM- benzalkonium chloride soap

  • NDC Code(s): 81792-002-01
  • 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 14, 2021

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  • Active Ingredient

    Benzalkonium Cloride 0.13%

  • Purpose

    Antimicrobial

  • Uses:

    For handwashing to decrease bacteria on the skin.

    Recommended for repeated use.

  • Warnings:

    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 if condition persists for more than 72 hours.

    Keep out of reach of Children.

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

  • Directions:

    Pump a small amount of foam into palm of hand.

    Rub thoroughly over all surfaces of both hands for 15 seconds.

    Rinse with potable water.

  • Other Information:

    Store at 20 to 25C. (68-77F)

  • Inactive Ingredients:

    Water, Coco-Glucoside, Laurtrimonium Chloride, Cocamidopropylamine Oxide, Citric Acid.

  • PRINCIPAL DISPLAY PANEL

    TRANSCEND

    by VONDREHLE

    E2 SANITIZING FOAM

    SOAP WITH BAK

    Manufactured for von Drehle Corporation I Hickory, NC 28601

    QUESTIONS?

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

    NSF

    Nonfood Compounds

    Program Listed (E2)

    (Registration #000000)

    1

    PET

    Item #T700E2

    1250 ml (42 fl. oz.

    Made in the U.S. A.

    container label

  • INGREDIENTS AND APPEARANCE
    TRANSCEND E2 SANITIZING FOAM 
    benzalkonium chloride soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81792-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    COCO GLUCOSIDE (UNII: ICS790225B)  
    LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81792-002-011250 mL in 1 BOTTLE; Type 0: Not a Combination Product04/14/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/14/2021
    Labeler - Von Drehle Corporation (071054415)
    Establishment
    NameAddressID/FEIBusiness Operations
    Woodbine Products Company004220323manufacture(81792-002)
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