Label: LEXI WHITE BEAUTY 5% MINOXIDIL SERUM- minoxidil liquid
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NDC Code(s):
83566-401-01,
83566-401-02,
83566-401-03,
83566-401-04, view more83566-401-05, 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.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
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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
- DO NOT USE
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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
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LEXI WHITE BEAUTY 5% MINOXIDIL SERUM
minoxidil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83566-401 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) PROPYLENE (UNII: AUG1H506LY) BIOTIN (UNII: 6SO6U10H04) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83566-401-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 2 NDC:83566-401-02 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 3 NDC:83566-401-03 80 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 4 NDC:83566-401-04 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 5 NDC:83566-401-05 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 6 NDC:83566-401-06 150 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 7 NDC:83566-401-07 180 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 8 NDC:83566-401-08 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 9 NDC:83566-401-09 220 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/08/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/08/2024 Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107) Establishment Name Address ID/FEI Business Operations Guangdong Aimu Biological Technology Co., Ltd 712647107 manufacture(83566-401)