Label: 5%MINOXIDIL HAIR GROWTH SPRAYS SERUM- minoxidil liquid

  • NDC Code(s): 84355-004-01
  • Packager: Guangzhou Binsi Clothing Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 20, 2026

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Minoxidil 5%

  • PURPOSE

    Hair regrowth treatment

  • INDICATIONS & USAGE

    Use to regrow hair on the scalp

  • WARNINGS

    For external use only.

  • DO NOT USE

    on a broken or irritated scalp.
    if you are allergic to any of the ingredients.
    if you are pregnant or nursing, or have any underlying medical condition, consult a healthcare provider before use.

  • WHEN USING

    avoid contact with eyes. In case of contact, rinse thoroughly with water.

  • STOP USE

    you experience headache, scalp redness,swelling, nausea, dizziness, or other adverse reactions.

  • KEEP OUT OF REACH OF CHILDREN

    if swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    use the dropper to apply a few drops to areas of hair loss on the scalp. Gently massage with fingertips for 3-5 minutes until fully absorbed.
    using more product or applying it more
    frequently will not improve results. Continued
    use is required to help maintain hair regrowth;
    otherwise, hair loss may resume.

  • INACTIVE INGREDIENT

    PROPYLENE GLYCOL
    AQUA
    ALCOHOL
    BUTYLENE GLYCOL
    CAFFEINE
    NIACINAMIDE
    CITRIC ACID
    ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL
    CYCLODEXTRIN
    MENTHOLUM
    HYDROXYPHENYL PROPAMIDOBENZOIC ACID
    PAEONIA SUFFRUTICOSA ROOT BARK EXTRACT
    PAEONIA ALBIFLORA ROOT EXTRACT
    CHRYSANTHEMUM INDICUM FLOWER EXTRACT

  • PRINCIPAL DISPLAY PANEL

    label1

    label

  • INGREDIENTS AND APPEARANCE
    5%MINOXIDIL HAIR GROWTH SPRAYS SERUM 
    minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84355-004
    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
    MENTHOL (UNII: L7T10EIP3A)  
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CYCLODEXTRIN (UNII: 7E6SK9QDT8)  
    ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL (UNII: 8LGU7VM393)  
    ALCOHOL (UNII: 3K9958V90M)  
    AQUA (UNII: 059QF0KO0R)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    CAFFEINE (UNII: 3G6A5W338E)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    CITRIC ACID (UNII: 2968PHW8QP)  
    PAEONIA SUFFRUTICOSA ROOT BARK (UNII: BUG255FE7X)  
    CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)  
    HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84355-004-011 in 1 BOX03/04/2025
    160 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/04/2025
    Labeler - Guangzhou Binsi Clothing Co.,Ltd. (418211411)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Binsi Clothing Co.,Ltd.418211411manufacture(84355-004)