Label: PLANEAIRE HANDS- ethanol hand sanitizer gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 20, 2023

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  • Active Ingredient(s)

    Ethyl 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 on hands. Flammable. Keep away from heat and flame

  • Do not use

    • on open skin 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 condition persists for more than 72 hours, consult a doctor.

    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

    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 inner leaf, carbomer, glycerin, green tea extract, mint oil fragrance blend , sodium hydroxide, water

  • Package Label - Principal Display Panel

    PAH Label 80335-112-0260 mL NDC: 80335-112-02

  • INGREDIENTS AND APPEARANCE
    PLANEAIRE HANDS 
    ethanol hand sanitizer gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80335-112
    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
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)  
    SPEARMINT (UNII: J7I2T6IV1N)  
    MINT (UNII: FV98Z8GITP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80335-112-0260 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/11/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/11/2021
    Labeler - EverywhereAire LLC (117635273)
    Registrant - EverywhereAire LLC (117635273)
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