Label: FYMIOX MINOXIDIL HAIR GROWTH SPRAY.- minoxidil hair growth spray. spray

  • NDC Code(s): 84213-001-01, 84213-001-02
  • Packager: Shenzhen Weilaiwang Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 27, 2024

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

  • Active Ingredient

    Minoxidil 5%

  • Purpose

    Hair Growth

  • Use

    Helps hair growth

  • Warnings

    For external use only

  • Do not use

    Do not use on injured skin

  • When Using

    When using this product,Avoid to contact with eyes.In case of accidental contact,clean and rinse eyes with large amounts of cool tap-water immediately.

  • Stop Use

    Stop use and ask doctor if irritation or rash appears and lasts.

  • Ask Doctor

    Changes in hair color or texture may happen to some persons.

  • Keep Oot Of Reach Of Children

    The amount of hair regrowth is various for each person.This product will not work for all persons.
    Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

  • Directions

    Use the spray head to apply the serum to the scalp in the area of thinning
    Please do an allergy test before use

  • Other information

    Please do an allergy test before use

  • Inactive ingredients

    Water, Butanediol, Phenoxyaethanolum, Hyaluronic acid, VB5, Platycladus orientalis leaf extract, Ginger root extract, Polygonum multiflorum extract

  • PRINCIPAL DISPLAY PANEL

    12

  • INGREDIENTS AND APPEARANCE
    FYMIOX MINOXIDIL HAIR GROWTH SPRAY. 
    minoxidil hair growth spray. spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84213-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTANEDIOL (MIXED ISOMERS) (UNII: TMS4MGA0H4)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    GINGER (UNII: C5529G5JPQ)  
    REYNOUTRIA MULTIFLORA ROOT OIL (UNII: 1HIE915O2J)  
    PLATYCLADUS ORIENTALIS LEAF (UNII: 32E5V7G32B)  
    PANTOTHENIC ACID (UNII: 19F5HK2737)  
    ANISOLE (UNII: B3W693GAZH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84213-001-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2024
    2NDC:84213-001-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03203/28/2024
    Labeler - Shenzhen Weilaiwang Technology Co., Ltd (705168691)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Weilaiwang Technology Co., Ltd705168691manufacture(84213-001) , label(84213-001)