Label: BEARD GROWTH SOLUTION liquid

  • NDC Code(s): 84117-006-01
  • Packager: Shenzhen Hengkaifeng Commerce and Trade Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 25, 2024

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

View All Sections
  • ACTIVE INGREDIENT

    Minoxidil 5%

  • Purpose

    Beard Regrowth Treatment

  • Use

    Beard growth solution to help
    firming hair root and balancing the facial
    skin secretion, improve the beard itching,
    remove the grease, clear the hair follicles
    to promote the beard growth, reduce the
    hair loss and broken hair, give you a
    healthy beard looks.

  • Warnings

    For adult external use only. Flammable.
    Keep away from heat or flame
    Do not use
    * Pregnant women and children.
    * on open skin wounds

  • When Using

    When using this product keep out of
    eyes, ears, and mouth, In case of contact
    with eyes,rinse eyes thoroughly with
    water. Stop use and ask a doctor if
    irritation or rash occurs. These may be
    signs of a serious condition.Keep out of
    reach of children. If swallowed, get
    medical help or contact a Poison Control
    Center right away.

  • Keep Out Of Reach Of Children

    Keep Out Of Reach Of Children

  • Directions Of Safe Use:

    * Put right amount of beard growth solu-
    tion apply on the beard loss area or facial
    hair, gentle to massage to help absorb.
    * 1-2 times per day.

  • Other information

    Store between15-30C(59-86F)
    Avoid freezing and excessive heat above
    40C (104F)

  • Inactive ingredients

    Aqua, Vitamin E Nicotinate,Argan Oil
    PEG-8 Esters,Caffeine, Rosemary Leaf oil,
    Ginger Root oil,Sage Oil, Simmondsia
    Chinensis (Jojoba) Seed Oil, Biotin.

  • DOSAGE & ADMINISTRATION

  • PRINCIPAL DISPLAY PANEL

    010203

  • INGREDIENTS AND APPEARANCE
    BEARD GROWTH SOLUTION 
    beard growth solution liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84117-006
    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)  
    TOCOPHERYL NICOTINATE (UNII: WI1J5UCY5C)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    CAFFEINE (UNII: 3G6A5W338E)  
    ROSEMARY OIL (UNII: 8LGU7VM393)  
    GINGER OIL (UNII: SAS9Z1SVUK)  
    SAGE OIL (UNII: U27K0H1H2O)  
    JOJOBA OIL (UNII: 724GKU717M)  
    BIOTIN (UNII: 6SO6U10H04)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84117-006-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product04/25/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03204/25/2024
    Labeler - Shenzhen Hengkaifeng Commerce and Trade Co., Ltd (444722774)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Hengkaifeng Commerce and Trade Co., Ltd444722774manufacture(84117-006) , label(84117-006)
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!