Label: LEXI WHITE BEAUTY HAIR REGROWTH 5% MINOXIDILSPRAY- minoxidil liquid
-
NDC Code(s):
83566-403-01,
83566-403-02,
83566-403-03,
83566-403-04, view more83566-403-05, 83566-403-06, 83566-403-07, 83566-403-08, 83566-403-09, 83566-403-10
- 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. ln case of accidental contact, rinse eyse 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
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LEXI WHITE BEAUTY HAIR REGROWTH 5% MINOXIDILSPRAY
minoxidil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83566-403 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) WATER (UNII: 059QF0KO0R) CAFFEINE (UNII: 3G6A5W338E) GLYCERIN (UNII: PDC6A3C0OX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) BIOTIN (UNII: 6SO6U10H04) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83566-403-01 1 in 1 BOX 01/23/2024 1 30 mL in 1 CANISTER; Type 0: Not a Combination Product 2 NDC:83566-403-02 1 in 1 BOX 01/23/2024 2 50 mL in 1 CANISTER; Type 0: Not a Combination Product 3 NDC:83566-403-03 1 in 1 BOX 01/23/2024 3 60 mL in 1 CANISTER; Type 0: Not a Combination Product 4 NDC:83566-403-04 1 in 1 BOX 01/23/2024 4 80 mL in 1 CANISTER; Type 0: Not a Combination Product 5 NDC:83566-403-05 1 in 1 BOX 01/23/2024 5 100 mL in 1 CANISTER; Type 0: Not a Combination Product 6 NDC:83566-403-06 1 in 1 BOX 01/23/2024 6 120 mL in 1 CANISTER; Type 0: Not a Combination Product 7 NDC:83566-403-07 1 in 1 BOX 01/23/2024 7 150 mL in 1 CANISTER; Type 0: Not a Combination Product 8 NDC:83566-403-08 1 in 1 BOX 01/23/2024 8 180 mL in 1 CANISTER; Type 0: Not a Combination Product 9 NDC:83566-403-09 1 in 1 BOX 01/23/2024 9 200 mL in 1 CANISTER; Type 0: Not a Combination Product 10 NDC:83566-403-10 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(83566-403)