Label: DRUGGIST 5% MINOXIDIL- 5% minoxidil liquid

  • NDC Code(s): 83872-261-01
  • Packager: Shenzhen Xiaomai Manufacturing Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 26, 2024

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

  • Active Ingredient

    Minoxidil 5%


    Biotin 10%

  • Purpose

    Effectively stimulate stronger and later hair growth .

  • Use

    Use to regrow hair on the top of the scalp

  • Warnings

    For external use only
    Do not use on damaged or broken skin
    When using this product keep out of eyes. Rinse with water to remove.
    Stop use and ask a doctor if rash occurs
    Keep out of reach of children.If swallowed, get medical help or contacta Poison Control Center right away.

  • Do not use

    Do not use on damaged or broken skin

  • When Using

    When using this product keep out of eyes. Rinse with water to remove.

  • Stop Use

    Stop use and ask a doctor if rash occurs

  • Keep Oot Of Reach Of Children

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

  • Ask Doctor

    Stop use and ask a doctor if rash occurs

  • Directions

    1. Apply 1 ML(few drops) directly onto scalp on the hair loss area.
    2. Use fingertips to massage solution into skin/hair for2-3 minutes.
    3 . Allow time for hair to fully absorb Growth Oil Forbest results, use twice daily on clean dry hair.

  • Other information

    Please store in a cool, dry place away from direct sunlight.

  • Inactive ingredients

    Hydrolyzed Ginseng Root,Angelica Sinensis Root Oil,Polygonum Multiflorum Extract,Ligustrum Vulgare Fruit Extract,Ligusticum Chuanxiong Extract,Carthamus Tinctorius (Safflower) Flower ExtractGlycyrrhiza Uralensis (Licorice) Callus Extract.

  • Purpose

    Hair Regrowth Treatment

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    DRUGGIST 5% MINOXIDIL 
    5% minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83872-261
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN10 g  in 30 mL
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL5 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    LIGUSTRUM VULGARE WHOLE (UNII: FC604DJ98E)  
    ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30)  
    CARTHAMUS TINCTORIUS FLOWER OIL (UNII: SDQ136WIM5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83872-261-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product06/26/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)06/26/2024
    Labeler - Shenzhen Xiaomai Manufacturing Co., Ltd. (712999147)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Xiaomai Manufacturing Co., Ltd.712999147manufacture(83872-261)