Label: YESUL HAND SANITIZER WIPES- benzalkonium chloride cloth

  • 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 July 28, 2020

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

View All Sections
  • ACTIVE INGREDIENT

    benzalkonium chloride

  • INACTIVE INGREDIENT

    water, glycerin, polysorbate 80, sodium benzoate, benzalkonium chloride, citric acid, maltodextrin, aloe barbadensis leaf juice powder, limonene, tocopheryl acetate, linalool, citral, citronellol, geraniol, benzyl benzoate, benzyl salicylate, farnesol, eugenol, isoeugenol, benzyl alcohol, fragrance

  • PURPOSE

    Antiseptic

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Wipe hands thoroughly with product and allow to dry.

    Discard wipe in trash. Do not flush.

  • WARNINGS

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

    When using this product keep out of eyes. in case of contact with eyes, flush thoroughly with water.

    avoid contact with broken skin.

    do not inhale or ingest.

    Stop use and ask a doctor if irritation and redness develop. 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.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    YESUL HAND SANITIZER WIPES 
    benzalkonium chloride cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76966-0014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1677 g  in 50 
    Inactive Ingredients
    Ingredient NameStrength
    CITRAL (UNII: T7EU0O9VPP)  
    GERANIOL (UNII: L837108USY)  
    BENZYL SALICYLATE (UNII: WAO5MNK9TU)  
    FARNESOL (UNII: EB41QIU6JL)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    EUGENOL (UNII: 3T8H1794QW)  
    ISOEUGENOL (UNII: 5M0MWY797U)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76966-0014-150 in 1 PACKAGE; Type 0: Not a Combination Product06/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/15/2020
    Labeler - N Bridge Inc. (694892752)
    Registrant - N Bridge Inc. (694892752)
    Establishment
    NameAddressID/FEIBusiness Operations
    WOOIL C&TECH.CORP688331078manufacture(76966-0014)
    Establishment
    NameAddressID/FEIBusiness Operations
    N Bridge Inc.694892752label(76966-0014)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!