Label: PLANEAIRE HANDS- hand sanitizer ethanol-based lotion

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

Drug Label Information

Updated December 20, 2023

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  • Purpose

    Antiseptic

  • ACTIVE INGREDIENT

    Ethyl alcohol 70 % v/v

  • INDICATIONS & USAGE

    • helps 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 wounds or near eyes. In case of contact with eyes, rinse thoroughly with watwer.

    Discontinue Use if

    • irritation or redness develops
    • If cindiction 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.

  • 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 15-30 C (59-86 F)
    • do not store above 105 F
    • avoid freezing
    • may discolor some fabrics
    • may be harmful to some wood finishes and plastics
  • Other Information

    • store between 15-30 C
    • do not store above 105 F
    • avoid freezing
    • may discolor some fabrics
    • may be harmful to some wood finishes and plastics
  • Inactive Ingredients

    Aloe Vera (Inner Leaf), Chlorella Vulgaris Powder, Glycerin, Green Tea Extract ( Camellia Sinensis Leaf), Lemongrass (Cymbopogon Schoenanthus) Oil, Lingonberry ( Vaccinium Vitis-Idaea) Seed Oil, Polyacrylate Crosspolymer-6, Rosemary (Rosmarinus Officinalis) Leaf Oil, Safflower Seed Oil ( Carthamus Tinctorius), Spirulina Platensis Powder, Water (Aqua)

  • Package Label

    80335-116

  • INGREDIENTS AND APPEARANCE
    PLANEAIRE HANDS 
    hand sanitizer ethanol-based lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80335-116
    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
    WATER (UNII: 059QF0KO0R)  
    SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE)  
    ALOE VERA LEAF POLYSACCHARIDES (UNII: W21O437517)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)  
    LINGONBERRY SEED OIL (UNII: 44P1VFO6KM)  
    CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80335-116-0260 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product10/24/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/24/2022
    Labeler - EverywhereAire LLC (117635273)
    Registrant - EverywhereAire LLC (117635273)
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