Label: LEXI WHITE BEAUTY HAIR REGROWTH 5% MINOXIDIL FOAM- minoxidil liquid
-
NDC Code(s):
83566-402-01,
83566-402-02,
83566-402-03,
83566-402-04, view more83566-402-05, 83566-402-06, 83566-402-07, 83566-402-08, 83566-402-09, 83566-402-10
- 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
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
-
WHEN USING
Do not apply on other parts of the body.
Avoid contact with eyes. In case of accidental contact,rinse evse with a large amount 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
Apply half a capful 2 times a day to the scalp in the hair loss area.
Massage into scalp with fingers, then wash hands well.
Using more hair regrowth foam or using the foam more will not improve your results.
Continued use is necessary to increase and then maintain your hair regrowth.
Discontinuing use may result in hair loss. - STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LEXI WHITE BEAUTY HAIR REGROWTH 5% MINOXIDIL FOAM
minoxidil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83566-402 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 0.05 g in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) CAFFEINE (UNII: 3G6A5W338E) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BIOTIN (UNII: 6SO6U10H04) POLYSORBATE 20 (UNII: 7T1F30V5YH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83566-402-01 1 in 1 BOX 01/23/2024 1 30 mL in 1 CANISTER; Type 0: Not a Combination Product 2 NDC:83566-402-02 1 in 1 BOX 01/23/2024 2 50 mL in 1 CANISTER; Type 0: Not a Combination Product 3 NDC:83566-402-03 1 in 1 BOX 01/23/2024 3 60 mL in 1 CANISTER; Type 0: Not a Combination Product 4 NDC:83566-402-04 1 in 1 BOX 01/23/2024 4 80 mL in 1 CANISTER; Type 0: Not a Combination Product 5 NDC:83566-402-05 1 in 1 BOX 01/23/2024 5 100 mL in 1 CANISTER; Type 0: Not a Combination Product 6 NDC:83566-402-06 1 in 1 BOX 01/23/2024 6 120 mL in 1 CANISTER; Type 0: Not a Combination Product 7 NDC:83566-402-07 1 in 1 BOX 01/23/2024 7 150 mL in 1 CANISTER; Type 0: Not a Combination Product 8 NDC:83566-402-08 1 in 1 BOX 01/23/2024 8 180 mL in 1 CANISTER; Type 0: Not a Combination Product 9 NDC:83566-402-09 1 in 1 BOX 01/23/2024 9 200 mL in 1 CANISTER; Type 0: Not a Combination Product 10 NDC:83566-402-10 1 in 1 BOX 01/23/2024 10 220 mL in 1 CANISTER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 01/23/2024 Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107) Establishment Name Address ID/FEI Business Operations Guangdong Aimu Biological Technology Co., Ltd 712647107 manufacture(83566-402)