Label: HOPS ANTIBACTERIAL WET WIPES- benzalkonium chloride 0.10% cloth

  • NDC Code(s): 81990-001-01
  • Packager: Sapro Temizlik Urunleri Sanayi ve Ticaret Anonim Sirketi
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 30, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredient(s)

    Alcohol 80% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

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

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • 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.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients

    glycerin, hydrogen peroxide, purified water USP

  • PRINCIPAL DISPLAY PANEL

    Product label image

  • INGREDIENTS AND APPEARANCE
    HOPS ANTIBACTERIAL WET WIPES 
    benzalkonium chloride 0.10% cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81990-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 U  in 100 U
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674) 0.12 U  in 100 U
    DEHYDROACETIC ACID (UNII: 2KAG279R6R) 0.068 U  in 100 U
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.01 U  in 100 U
    PHENOXYETHANOL (UNII: HIE492ZZ3T) 0.68 U  in 100 U
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.5 U  in 100 U
    WATER (UNII: 059QF0KO0R) 98.02 U  in 100 U
    BENZOIC ACID (UNII: 8SKN0B0MIM) 0.102 U  in 100 U
    SODIUM GLUCONATE (UNII: R6Q3791S76) 0.1 U  in 100 U
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) 0.05 U  in 100 U
    Product Characteristics
    Color    Score    
    ShapeRECTANGLE (Wet wipes) Size
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81990-001-0160 U in 1 POUCH; Type 0: Not a Combination Product07/01/2021
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/01/2021
    Labeler - Sapro Temizlik Urunleri Sanayi ve Ticaret Anonim Sirketi (365536965)
    Registrant - Sapro Temizlik Urunleri Sanayi ve Ticaret Anonim Sirketi (365536965)
    Establishment
    NameAddressID/FEIBusiness Operations
    Sapro Temizlik Urunleri Sanayi ve Ticaret Anonim Sirketi365536965manufacture(81990-001)