Label: ONIADBA 5% MINOXIDIL HAIR GROWTH SPRAYS SERUM- minoxidil 5% liquid
- NDC Code(s): 85992-001-01
- Packager: Shenzhen Boyimei Technology Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 10, 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 your eyes with large amounts of cool tap water.
Some people have experienced changes in hair color and/or texture.
lt takes time to regrow hair. Results may occur at 3 months with twice a day usage. For some men, you may need to use this product 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 your eyes with a large amount of cool tap water. - STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
1.Make sure your hair and scalp are completely dry before applying. (No need to wash your hair beforehand.)
2.Apply 3-4 sprays directly to the target area of the scalp.
3.Gently massage the product into your scalp or thinning areas until fully absorbed.
4.For best results, use consistenlly to boost and maintain hair regrowth, Stopping treatment may lead to hair loss returning. - INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ONIADBA 5% MINOXIDIL HAIR GROWTH SPRAYS SERUM
minoxidil 5% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85992-001 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 BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 0.005 g in 1 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DEXPANTHENOL (UNII: 1O6C93RI7Z) CASTOR OIL (UNII: D5340Y2I9G) ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85992-001-01 4 in 1 PACKAGE 07/10/2025 1 60 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) 07/10/2025 Labeler - Shenzhen Boyimei Technology Co., Ltd. (979497977) Establishment Name Address ID/FEI Business Operations Shenzhen Boyimei Technology Co., Ltd. 979497977 manufacture(85992-001)
