Label: AMBER OUD WOOD HAND SANITIZER liquid

  • NDC Code(s): 41366-091-01
  • Packager: Zhejiang Meimi Technology Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 10, 2025

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  • Active Ingredient(s)

    Ethyl Alcohol 70% v/v

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help reduce bacteria on the skin that may cause disease.

  • Warnings

    • for external use only.
    • Flammable.
    • Keep away from heat and flame.
  • STOP USE

    Stop use and ask a doctor if·irritation or redness develops.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children·
    if swallowed, get medical help or contact a Poison Control Center.

  • Directions

    Spray enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Recommended for repeated use. Children under 6 years of age should be supervised when using this product.

  • Inactive ingredients

    Water(Aqua), Fragrance(Parfum), Glycerin, Hexyl Cinnamal, Limonene, Linalool, Yellow 6, Blue 1, Yellow 5.

  • WHEN USING

    When using this product·
    avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

  • Package Label - Principal Display Panel

    45 mL in 1 BOTTLE

    NDC: 41366-091-01

    label

  • INGREDIENTS AND APPEARANCE
    AMBER OUD WOOD HAND SANITIZER 
    amber oud wood hand sanitizer liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41366-091
    Route of AdministrationEXTRACORPOREAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    HEXYL CINNAMAL (UNII: 7X6O37OK2I)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    BLUE 1 (UNII: H3R47K3TBD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    YELLOW 5 (UNII: I753WB2F1M)  
    LINALOOL (UNII: D81QY6I88E)  
    YELLOW 6 (UNII: H77VEI93A8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41366-091-0145 mL in 1 BOTTLE; Type 0: Not a Combination Product06/10/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00306/10/2025
    Labeler - Zhejiang Meimi Technology Co., Ltd. (413668440)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Meimi Technology Co., Ltd.413668440manufacture(41366-091)
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