Label: ANYASK 5% MINOXIDIL HAIR GROWTH SERUM WITH BIOTIN- minoxidil liquid

  • NDC Code(s): 84450-001-01
  • Packager: Shenzhen Dong bu luo Technology Co., LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 25, 2024

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

  • Active ingredients

    5% Minoxidil

  • PURPOSE

    Hair Regrowth Treatment

  • USE

    HELP HAIR GROWTH

  • WARNINGS

    For external use only

    Avoid contact with eyes

    When using

    This product is for topical use on the scalp only and should not betaken orally or applied to other areas of the body. Avoid contact with the eyes.

    Stop use

    If your scalp is allergic to this product, red, inflamed, infected or irritated, stop useing it immediately.

    Do not use

    May be harmful during pregnant or breast-feeding.

    Keep out of reach of children

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

  • DIRECTIONS

    The total daily dose should NOT exceed 3ml. Men should use it once in the morning and once in the evening, while women should use it once a day

    Apply 1ml of Minoxidil solution to the scalp, starting from the center,and massage with hands for 3-5minutes.

  • INACTIVE INGREDIENTS

    Water, Glycerol, Gleditsia sinensis seed extract, Polygonum multiflorum extract, Kochia scoparia extract, Biota orientalis leaf extract, Phryma leptostachya extract, Syringa oblata extract, Chrysanthemum parthenium (feverfew) extract, Dictamnus dasycarpus root bark extract, Sorbic acid, Phenoxyethanol, Biotin

  • PRINCIPAL DISPLAY PANEL

    1213

  • INGREDIENTS AND APPEARANCE
    ANYASK 5% MINOXIDIL HAIR GROWTH SERUM WITH BIOTIN 
    minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84450-001
    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
    GLEDITSIA SINENSIS SEED (UNII: T651YZ712C)  
    BIOTIN (UNII: 6SO6U10H04)  
    DICTAMNUS DASYCARPUS ROOT BARK (UNII: LA97176ILS)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BASSIA SCOPARIA WHOLE (UNII: 240G38P85Z)  
    SYRINGA OBLATA WHOLE (UNII: T272Z8620J)  
    WATER (UNII: 059QF0KO0R)  
    REYNOUTRIA MULTIFLORA WHOLE (UNII: 85S46HFR8A)  
    PHRYMA LEPTOSTACHYA WHOLE (UNII: 6G287VJM69)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TANACETUM PARTHENIUM WHOLE (UNII: 6GE7Z0761K)  
    SORBIC ACID (UNII: X045WJ989B)  
    PLATYCLADUS ORIENTALIS LEAF (UNII: 32E5V7G32B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84450-001-0160 mL in 1 BOTTLE; Type 0: Not a Combination Product06/25/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03206/25/2024
    Labeler - Shenzhen Dong bu luo Technology Co., LTD (614263505)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Dong bu luo Technology Co., LTD614263505manufacture(84450-001)