Label: 2% MINOXIDIL HAIR GROWTH SERUM- 2% minoxidil liquid

  • NDC Code(s): 84693-001-01
  • Packager: Zonnsmart Science & Technology Co.,Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 29, 2024

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

  • ACTIVE INGREDIENT

    Minoxidil 2%

  • PURPOSE

    ANTI HAIR LOSS, HAIR STRENGTHENING

  • KEEP OUT OF REACH OF CHILDREN

    Please keep it out of reach of children.

  • INDICATIONS & USAGE

    ANTI HAIR LOSS, HAIR STRENGTHENING, EASY TO USE

  • WARNINGS

    1. For extemal use only. Avoid contact witheyes. Please keep it out of reach of children.Seal the product and avoid light store in acool and dry place.

  • DOSAGE & ADMINISTRATION

    1. Before using the product, it is necessaryto clean the scalp and skin;
    2. Best result with a scalp applicator thatincluded in the gift box
    3. For male: Pour about 2ml of hair oil intothe scalp applicator(Once a day);For female: Pour about 1ml of hair oilinto the scalp applicator (Once a day);
    4. Allow time for hair to fully absorb serum;do not dry;
    5. For longer hair;to obtain maximumabsorption, wrap hair together in a bun andlet soak.

  • STORAGE AND HANDLING

    Seal the product and avoid light store in acool and dry place.

  • INACTIVE INGREDIENT

    PHENOXYETHANOL
    ETHYLHEXYLGLYCERIN
    DISODIUM EDTA
    WATER
    ALCOHOL
    PROPYLENE GLYCOL
    BUTYLENE GLYCOL

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    2% MINOXIDIL HAIR GROWTH SERUM 
    2% minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84693-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84693-001-011 in 1 BOX08/30/2024
    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)08/30/2024
    Labeler - Zonnsmart Science & Technology Co.,Ltd (714639269)
    Registrant - Zonnsmart Science & Technology Co.,Ltd (714639269)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zonnsmart Science & Technology Co.,Ltd714639269manufacture(84693-001)