Label: FOR HAIR MINOXIDIL BIOTIN HAIR SERUM- minoxidil biotin hair serum liquid
- NDC Code(s): 83872-058-01
- Packager: Shenzhen XiaoMai Manufacturing Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 19, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- Uses
- WARNINGS
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Do not use
You have no family history of hair loss,hair loss is sudden and/or patchy.
You do not know the reason for you hair loss.
You ae under 18 years of age, Do not use it on babies and children your scalp is red,inflamed,infected, irritated, or painful.
You use other medicines on the scalp.Ask a doctor before use if you hace heart disease. -
When using this product
Do not apply to other parts of the body, void contact with eyes, In case of accidental contact, rinse eyes with a large amount of cool tap water.
It takes time to regrow hair, You may need to usethis product 2 times a day for a least 4 monthsbefore you see results, The amount of hairregrowth is different for each preson. - Stop use and ask a doctor
- Keep out of reach of children.
- Directions for use
- Other Information
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
FOR HAIR MINOXIDIL BIOTIN HAIR SERUM
minoxidil biotin hair serum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83872-058 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 350 mg in 1 g MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 50 mg in 1 g CAFFEINE (UNII: 3G6A5W338E) (CAFFEINE - UNII:3G6A5W338E) CAFFEINE 350 mg in 1 g Inactive Ingredients Ingredient Name Strength BIOTIN (UNII: 6SO6U10H04) 250 mg in 1 g Product Characteristics Color brown Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83872-058-01 30 g in 1 BOTTLE; Type 0: Not a Combination Product 03/19/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 03/19/2024 Labeler - Shenzhen XiaoMai Manufacturing Co., Ltd. (712999147) Establishment Name Address ID/FEI Business Operations Shenzhen XiaoMai Manufacturing Co., Ltd. 712999147 manufacture(83872-058)
