Label: HASOL INTENSIVE SCALP TONIC- salicylic acid, niacinamide, menthol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated August 20, 2014

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  • HA'SOL Intensive Scalp Tonic

    scalp tonic

    Salicylic acid (0.3%)
    Niacinamide (0.3%)
    Menthol (0.3%) 

    Antiseborrheic
    Hair tonic 

    Keep out of reach of children
    Do not swallow. In case of accidental ingestion, seek professional assistance.

    To recover the scalp condition for healthier hair. To strengthen hair root, give growth stimulation and thicken hair.

    For external use only

    Do not use when Your scalp is red, inflamed, irritated or painful

    When using this product
    Do not apply on other parts of the body
    Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
    Do not apply directly to wound or open cut.
    Stop use and ask doctor if rash or irritation on scalp develops and lasts.

    Store at room temperature 

    After shampoo, massage the scalp in order to be absorbed fully focusing on the part of hair loss. Do not rinse off after application since it is a hair loss preventing and hair tonic product.

    Water, Alcohol, PEG-60 Hydrogenated Castor Oil, Betaine, Camellia Sinensis Leaf Extract, Tribulus Terrestris Fruit Extract, Phyllanthus Emblica Fruit Extract, Panax Ginseng Root Extract, Tocopheryl Acetate, Fragrance, Salvia Officinalis (Sage) Extract, Serenoa Serrulata Fruit Extract, Urtica Dioica (Nettle) Extract, Equisetum Arvense Extract, Zingiber Officinale (Ginger) Root Extract, Laminaria Japonica Extract

  • INGREDIENTS AND APPEARANCE
    HASOL INTENSIVE SCALP TONIC 
    salicylic acid, niacinamide, menthol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51270-120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.3   in 100 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.3   in 100 mL
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.3   in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    BETAINE (UNII: 3SCV180C9W)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    TRIBULUS TERRESTRIS FRUIT (UNII: QNL076V6EQ)  
    PHYLLANTHUS EMBLICA FRUIT (UNII: YLX4CW2576)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SALVIA OFFICINALIS WHOLE (UNII: M9C36LC10E)  
    SAW PALMETTO (UNII: J7WWH9M8QS)  
    URTICA DIOICA LEAF (UNII: X6M0DRN46Q)  
    EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)  
    GINGER (UNII: C5529G5JPQ)  
    LAMINARIA JAPONICA (UNII: WE98HW412B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51270-120-021 in 1 CARTON
    1NDC:51270-120-01100 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/20/2014
    Labeler - ECOMINE Co., Ltd. (557795691)
    Registrant - ECOMINE Co., Ltd. (557795691)
    Establishment
    NameAddressID/FEIBusiness Operations
    ECOMINE Co., Ltd.557795691manufacture(51270-120)