Label: TRZSFR 5% MINOXIDIL HAIR GROWTH SPRAYS SERUM- minoxidil liquid
- NDC Code(s): 85304-011-01, 85304-011-02
- Packager: Guangzhou Borderless Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 5, 2025
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
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WHEN USING
Avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water
Some people have experienced changes in hair color and/or texture.
It takes time to regrow hair. Results may occur at 3 months with twice a day usage. For some men, you may need to use thisproduct for at least 6 months before you see results. The amount of hair regrowth is different for each person.
Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water.
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
-
DOSAGE & ADMINISTRATION
1.Make sure your hair and scalp are dry(no need to wash your hair before each use)
2.Apply 3-4 pumps of spray directly to the treated area of the scalp
3.Gently massage into the scalp or thinning hair areas until absorbed.
4.Continued use is reauired to increase and maintain hair regrowth. Discontinuation may lead to hair loss
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
TRZSFR 5% MINOXIDIL HAIR GROWTH SPRAYS SERUM
minoxidil liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85304-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 0.5 g in 100 mL MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1) MINOXIDIL 5 g in 100 mL Inactive Ingredients Ingredient Name Strength DEXPANTHENOL (UNII: 1O6C93RI7Z) WATER (UNII: 059QF0KO0R) CASTOR OIL (UNII: D5340Y2I9G) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85304-011-01 4 in 1 PACKAGE 08/05/2025 1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:85304-011-02 8 in 1 PACKAGE 08/05/2025 2 100 mL in 1 BOTTLE; 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) 08/05/2025 Labeler - Guangzhou Borderless Technology Co., Ltd. (452282332) Establishment Name Address ID/FEI Business Operations Guangzhou Borderless Technology Co., Ltd. 452282332 manufacture(85304-011)
