Label: LEXI WHITE BEAUTY 5% MINOXIDIL SERUM- minoxidil liquid

  • NDC Code(s): 83566-401-01, 83566-401-02, 83566-401-03, 83566-401-04, view more
    83566-401-05, 83566-401-06, 83566-401-07, 83566-401-08, 83566-401-09
  • Packager: Guangdong Aimu Biological Technology Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 15, 2024

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

  • SPL UNCLASSIFIED SECTION

    5% Minoxidil Serum

  • ACTIVE INGREDIENT

    Minoxidil 5%

  • PURPOSE

    Use to regrow hair on the scalp.

  • INDICATIONS & USAGE

    Apply 2-3 drops of serum directly on the scalp in the area to be treated.
    Massage into the scalp with your fingers then wash hands thoroughly.
    Using more hair regrowth serum or using the serum more often will not improve your results.
    Continued use is necessery to increase and then maintain your hair regrowth.
    Discontinuing use may result in hair loss.

  • WARNINGS

    For external use only

  • DO NOT USE

    You have no family history of hair loss, hair loss in sudden and/or patchy.
    You do not know the reason for your hair loss.
    You are under 18 years of age. Do not use it on babies and children.
    Scalp is red, inflamed, infected, irritated, or painful.
    You use other medicines on the scalp.

  • WHEN USING

    Do not apply on other parts of the body.
    Avoid contact with eyes. In case of accidental contact, rinse eyse with a largeamount of cool tap water.
    lt takes time to regrow hair. You may need to use this product 2 times a day for a least 4 months before you see results. The amount of hair regrowth is different for each person.
    The product will not work for everyone.

  • STOP USE

    Chest pain,rapid heart beat, faintness,or dizziness occurs.
    Sudden, unexplaind weight gain occurs.
    Your hands or feet swel.
    Scalp irritation or redness occurs.
    You get unwanted facial hair growth.
    You do not see hair regrowth in 4 months

  • KEEP OUT OF REACH OF CHILDREN

    lf swallowed, get medical help or contact a poison control center right away.

  • DOSAGE & ADMINISTRATION

    Apply 2-3 drops of serum directly on the scalp in the area to be treated.

    Massage into the scalp with your fingers then wash hands thoroughly.

  • STORAGE AND HANDLING

    Store at controlled room temperature 20 to 25°C (68 to 77°F).
    puncture or incinerate the container.Do not expose to heat or store at temperature above 120°F (49°C)

  • INACTIVE INGREDIENT

    Alcohol,propylene, purified water

  • PRINCIPAL DISPLAY PANEL

    label

    label2

  • INGREDIENTS AND APPEARANCE
    LEXI WHITE BEAUTY 5% MINOXIDIL SERUM 
    minoxidil liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83566-401
    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
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE (UNII: AUG1H506LY)  
    BIOTIN (UNII: 6SO6U10H04)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83566-401-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    2NDC:83566-401-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    3NDC:83566-401-0380 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    4NDC:83566-401-04100 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    5NDC:83566-401-05120 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    6NDC:83566-401-06150 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    7NDC:83566-401-07180 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    8NDC:83566-401-08200 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    9NDC:83566-401-09220 mL in 1 BOTTLE; Type 0: Not a Combination Product01/08/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)01/08/2024
    Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangdong Aimu Biological Technology Co., Ltd712647107manufacture(83566-401)