Label: PLANEAIRE HANDS SANDALWOOD- ethanol hand sanitizer lotion

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

Drug Label Information

Updated May 12, 2024

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  • Acttive Ingredient(s)

    Ethyl alcohol 70% v/v

  • Purpose

    Topical antiseptic

  • Use

    Hand Santizer to help reduce bacteria that potentially reduce disease. For us when soap and water are not available.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame.

  • Do not use

    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 condition 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
  • Storage and Handling

    • 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

  • Package label

    80335-118NDC 80335-118

  • INGREDIENTS AND APPEARANCE
    PLANEAIRE HANDS SANDALWOOD 
    ethanol hand sanitizer lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80335-118
    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
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    SANDALWOOD OIL (UNII: X7X01WMQ5F)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80335-118-0260 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2021
    Labeler - EverywhereAire LLC (117635273)
    Registrant - EverywhereAire LLC (117635273)
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