Label: PLANREAIRE HANDS HAND SANITIZER- ethyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 9, 2024

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  • Active Ingredient(s)

    Alcohol 70% v/v.

  • Purpose

    Antiseptic

  • 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

    • on open wounds or near eyes. In case of contact with eyes, rinse thoroughly with water
  • WHEN USING

    When using this product keep out of eyes. In case of contact with eyes, rinse eyes thoroughly with water.

    Stop use if irritation or rash occurs. If condtion persists for more than 72 hours, consult a doctor.

    Keep out of reach of children. If swallowed, get medical help or contact a local 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

    • Wet hands thoroughly with product, rub hands, and allow to dry without wiping.
    • For children under 6 years of age, use only under adult supervision to avoid swallowing
    • Not recommended for infants
  • Other information

    • Store between 15-30C (59-86F)
    • Do not store above 105F
    • Avoid freezing
    • may discolor some fabrics
    • may be harmful to some wood finishes and plastics
  • Inactive ingredients

    aloe vera, glycerin, green tea extract, polyacrylate crosspolymer-6, safflower seed oil, sandalwood fragrance blend, water

  • Package Label - Principal Display Panel

    PAH Label 80335-109-0260 mL NDC: 80335-109-02

  • INGREDIENTS AND APPEARANCE
    PLANREAIRE HANDS HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80335-109
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL80 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    SANDALWOOD OIL (UNII: X7X01WMQ5F)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80335-109-0260 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/21/2020
    Labeler - EverywhereAire LLC (117635273)
    Registrant - EverywhereAire LLC (117635273)
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