Label: NURI CARE HAND SANITIZING WIPES- hand sanitizing wipes cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

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 June 9, 2020

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  • Active Ingredient(s)

    Benzalkonium Chloride 0.1% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic

  • Use(s)

    Hand sanitizer to help reduce bacteria on the skin.

  • Warnings

    Children under 2 years ask a doctor before use.

  • 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

    Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

  • 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

    • Wet hands thoroughly with product and allow to dry
    • Supervise children under 6 years of age when using this product
  • Other information

    • Store at room temperature
  • Inactive ingredients

    Water, Sodium Hydroxide

  • Package Label - Principal Display Panel

    70 Sheets NDC: 75272-002-5070 Sheets NDC: 75272-002-50

  • INGREDIENTS AND APPEARANCE
    NURI CARE HAND SANITIZING WIPES 
    hand sanitizing wipes cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75272-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75272-002-50470 g in 1 PACKET; Type 0: Not a Combination Product05/13/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/13/2020
    Labeler - SUNJU CORPORATION (694816019)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nuricham, Inc.695541121manufacture(75272-002)
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