Label: 5% MINOXIDIL- minoxidil oil

  • NDC Code(s): 83889-101-01
  • Packager: Shenzhen Lancity Information Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated December 22, 2023

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

View All Sections
  • ACTIVE INGREDIENT

    Minoxidil 5%

  • PURPOSE

    Effective Solution
    ForHair Thinning And Breakage
    Make Hair Thicker Tealthier

  • KEEP OUT OF REACH OF CHILDREN

    Keep out ofreach of children

  • INDICATIONS & USAGE

    1.Keep scalp clean and dry before use
    2.Brush the hair and spray 6-7 times (about lml) on the scalp on the area of use
    3.Massage the affected area for 3-5 minutes to allow the solution to absorb thoroughly
    4.Wash hands after use to avoidcontamination with other items

  • WARNINGS

    1.External use, not internal, avoiddirect contact with the eyes, such asaccidentallyinto the eyes, that is,wash with water ;
    2. Keep out ofreach of children
    3. If you feelunwell, stop using it.

  • DOSAGE & ADMINISTRATION

    Brush the hair and spray 6-7 times (about lml) on the scalpon the area of use

  • STORAGE AND HANDLING

    Storage conditions: Please storein a cool and dry place to avoiddirect sunlight

  • INACTIVE INGREDIENT

    Water
    phenoxyethanol
    turmeric extract
    castor oil
    ginseng extract

  • PRINCIPAL DISPLAY PANEL

    labellabel2

  • INGREDIENTS AND APPEARANCE
    5% MINOXIDIL 
    minoxidil oil
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83889-101
    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
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    TURMERIC (UNII: 856YO1Z64F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83889-101-011 in 1 BOX12/22/2023
    160 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07535712/22/2023
    Labeler - Shenzhen Lancity Information Technology Co., Ltd (620465677)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lancity Information Technology Co., Ltd620465677manufacture(83889-101)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!