Label: ALLPURE HAND SANITIZER SANITIZING WIPE- alcohol cloth

  • NDC Code(s): 80176-001-01, 80176-001-02, 80176-001-03, 80176-001-04, view more
    80176-001-05, 80176-001-06
  • Packager: CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 31, 2023

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  • Active Ingredient

    Alcohol 70% v/v.

  • Purpose

    Antiseptic

  • Use

    Antiseptic wipe 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. Keep out of reach of children.

  • Do not use

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

    When using this productkeep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

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

  • STOP USE

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • Directions

    • Wet hands thoroughly with product and allow to dry without wiping.
    • 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, Butylene Glycol, Water, Lanolin

  • Package Label - Principal Display Panel

    Label

    Label 2

  • INGREDIENTS AND APPEARANCE
    ALLPURE HAND SANITIZER SANITIZING WIPE 
    alcohol cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80176-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LANOLIN (UNII: 7EV65EAW6H)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80176-001-011 in 1 PACKET08/20/2020
    15 mL in 1 POUCH; Type 0: Not a Combination Product
    2NDC:80176-001-0210 in 1 PACKET08/20/2020
    25 mL in 1 POUCH; Type 0: Not a Combination Product
    3NDC:80176-001-0350 in 1 PACKET08/20/2020
    35 mL in 1 POUCH; Type 0: Not a Combination Product
    4NDC:80176-001-0472 in 1 PACKET08/20/2020
    45 mL in 1 POUCH; Type 0: Not a Combination Product
    5NDC:80176-001-05120 in 1 PACKET08/20/2020
    55 mL in 1 POUCH; Type 0: Not a Combination Product
    6NDC:80176-001-06200 in 1 PACKET08/20/2020
    65 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/20/2020
    Labeler - CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI (502990784)
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