Label: MONPURIEL DAILY ALL IN ONE AMPLE- l-menthol, dexpanthenol, salicylic acid 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 January 4, 2024

If you are a consumer or patient please visit this version.

  • Active Ingredients

    L-Menthol 0.33%

    Dexpanthenol 0.22%

    Salicylic Acid 0.25%

  • Purposes

    L-Menthol 0.33%-------------------------------------- coolin

    Dexpanthenol 0.22%.............................................soothing

    Salicylic Acid 0.25%---------------------------------- exfoliating

  • Uses

    • helps scalp care for to prevent hair loss

    • if used as directed with other skin care measures, decreases the wrinkles and aging

  • Warnings

    For external use only

  • Warnings

    Do not use on damaged or broken skin

  • Warnings

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Warnings

    Stop use and ask a doctor if rash occurs

  • Warnings

    When using this product keep out of eyes.

  • Directions

    After cleansing and lightly preparing the skin with toner, take appropriate amount and apply to the skin, patting it in to absorb

  • Inactive Ingredients

    Dipropylene Glycol, Glycerin, Butylene Glycol, Water, 1,2-Hexanediol, Propanediol, Panthenol, Dipotassium Glycyrrhizate, Tromethamine, Xanthan Gum, Carbomer, PEG-60 Hydrogenated Castor Oil, Allantoin, Adenosine,

    Glyceryl Acrylate/Acrylic Acid Copolymer, Lavandula Angustifolia (Lavender) Oil (Allergens : Geraniol, Limonene, Linalool),

    Sodium Hyaluronate, Beta-Glucan, Phosphate buffered saline, Cynanchum Atratum Extract, Lactobacillus Extracellular Vesicles,

    sh-Oligopeptide-1, Ethylhexylglycerin, Lycium Chinense Fruit Extract

  • Label

    Daily all in one ample

  • INGREDIENTS AND APPEARANCE
    MONPURIEL DAILY ALL IN ONE AMPLE 
    l-menthol, dexpanthenol, salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83472-311
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL0.33 g  in 100 mL
    DEXPANTHENOL (UNII: 1O6C93RI7Z) (DEXPANTHENOL - UNII:1O6C93RI7Z) DEXPANTHENOL0.22 g  in 100 mL
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.25 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    LACTOBACILLUS ACIDOPHILUS (UNII: 1PRR1V42V5)  
    CENTELLA ASIATICA LEAF (UNII: 6810070TYD)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    TROMETHAMINE (UNII: 023C2WHX2V)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    ALLANTOIN (UNII: 344S277G0Z)  
    ADENOSINE (UNII: K72T3FS567)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER (300000 CP AT 2%) (UNII: MEA9KH24QG)  
    SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP)  
    LYCIUM CHINENSE FRUIT (UNII: TG711Q7A1Q)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    VINCETOXICUM ATRATUM WHOLE (UNII: U3176B0S5J)  
    NEPIDERMIN (UNII: TZK30RF92W)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83472-311-0130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product05/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/01/2023
    Labeler - Y2K Co., Ltd. (695705051)
    Registrant - Y2K Co., Ltd. (695705051)
    Establishment
    NameAddressID/FEIBusiness Operations
    Y2K Co., Ltd.695705051manufacture(83472-311)