Label: HAND SANITIZER GEL- alcohol gel

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

Drug Label Information

Updated December 21, 2023

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  • Active Ingredient(s)

    Ethyl Alcohol 70% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic,

  • Use

    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 or flame

  • Do not use

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

    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, cnsukt 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 if irritation or rash occurs. If condition persists for more than 72 hours, consult a doctor.

  • KEEP OUT OF REACH OF CHILDREN

    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 15-30C (59-86F)
    • Do not store above 105F
    • Avoid freezing
    • May discolor some fabrics
    • May be harmful tio some wood finishes and plastics

    Inactive ingredients

    Aloe Vera (Inner leaf)
    Basil (Ocimum Basilicum) Leaf Extract
    Chlorella Vulgaris Powder
    Glycerin
    Green tea (Camellia Sinensis) Leaf Extract
    Lingonberry (Vaccinium Vitis-Idaea) Seed Oil
    Polyacrylate Crosspolymer-6
    Pomegranate (Punica Granatum) seed oil
    Pomegranate fragrance
    Safflower (Carthamus Tinctorius ) seed oil
    Spirulina Platensis Powder
    Water

  • Package Label - Principal Display Panel NDC 80335-114-02

    80335-114-02​NDC: 80335-114Pomegranate Basil hand sanitizer gel 80335-114-02

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER GEL 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80335-114
    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
    CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FRAGRANCE 13576 (UNII: 5EM498GW35)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BASIL (UNII: 2U0KZP0FDW)  
    POMEGRANATE SEED OIL (UNII: 0UI45XV0T6)  
    WATER (UNII: 059QF0KO0R)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    SAFFLOWER OIL (UNII: 65UEH262IS)  
    LINGONBERRY SEED OIL (UNII: 44P1VFO6KM)  
    SPIRULINA PLATENSIS (UNII: 9L3TIH1UUE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80335-114-0260 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product01/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/01/2022
    Labeler - EverywhereAire LLC (117635273)
    Registrant - EverywhereAire LLC (117635273)
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