Label: DR. C. TUNA ANTIBACTERIAL LIQUID HAND SANITIZER LEMON- alcohol liquid

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

Drug Label Information

Updated November 5, 2023

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  • Drug Facts

  • Active Ingredient

    Ethyl Alcohol 80% v/v

    Purpose

    Antiseptic

  • Use[s]

    Liquid Hand Sanitizer helps to reduce bacteria on the skin.

  • Warnings

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

    Do not use

    • on children under 2 months of age
    • on irritated and open skin wounds

    When using this product

    keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

    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.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30ºC ( 59-86ºF )
    • Avoid freezing and excessive heat above 40ºC (104ºF)
  • Inactive ingredients:

    Water/Aqua, Fragrance/Parfum, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Juice, Citral, Limonene, Linalool.

  • Package Labeling:

    Bottle

  • INGREDIENTS AND APPEARANCE
    DR. C. TUNA ANTIBACTERIAL LIQUID HAND SANITIZER LEMON 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74690-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.8 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CITRAL (UNII: T7EU0O9VPP)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:74690-007-011 in 1 BOX12/01/2020
    1115 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)12/01/2020
    Labeler - Farmasi US LLC (113303351)
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