Label: NEUROTOX HAND NEURO- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 6, 2020

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  • PRINCIPAL DISPLAY PANEL

    1

    Antiseptic

    Alcohol

    Water, Ferulic Acid, Gallic Acid, sh Decapeptide 7, sh Octapeptide 4, sh Oligopeptide
    9, sh Pentapeptide 19, Diospyros Kaki Leaf Extract, Vitis Vinifera (Grape) Fruit Extract, Coffea Arabica (Coffee) Seed Extract, Carthamus Tinctorius (Safflower) Flower Extract, Polygonum Cuspidatum Root Extract, Camellia Sinensis Leaf Extract, Castanea Crenata (Chestnut) Shell Extract, Zanthoxylum Piperitum Fruit Extract, Butylene Glycol, Carbomer, Tromethamine, 1,2 Hexanediol, Fragrance

    For the external use only

    .• Flammable. Keep away from fire or flame.
    • For external use only.
    • When using this product do not use in or near the eyes.
    In case of contact, rinse eyes thoroughly with water.
    • Stop use and ask a doctor if irritation or rash appears
    and lasts.
    • Keep Out of Reach of Children.
    • Do not eat.
    • If swallowed, get medical help or contact a Poison Control
    Center right away

    Directions
    • Put enough product in your palm to cover hands and rub
    hands together briskly until dry.
    • Children under 6 years of age should be supervised when
    using. Not recommended for infants.

    Keep out of reach of children

  • INGREDIENTS AND APPEARANCE
    NEUROTOX HAND NEURO 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76882-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL37.2 mL  in 60 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    WATER (UNII: 059QF0KO0R)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76882-0002-160 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/01/2020
    Labeler - BIO-FD&C. Co., Ltd. (688203268)
    Registrant - BIO-FD&C. Co., Ltd. (688203268)
    Establishment
    NameAddressID/FEIBusiness Operations
    BIO-FD&C. Co., Ltd.688203268manufacture(76882-0002)
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