FYMIOX MINOXIDIL HAIR GROWTH SPRAY.- minoxidil hair growth spray. spray

Fymiox Minoxidil Hair Growth Spray. by

Drug Labeling and Warnings

Fymiox Minoxidil Hair Growth Spray. by is a Otc medication manufactured, distributed, or labeled by Shenzhen Weilaiwang Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Minoxidil 5%

Purpose

Hair Growth

Use

Helps hair growth

Warnings

For external use only

Do not use

Do not use on injured skin

When Using

When using this product,Avoid to contact with eyes.In case of accidental contact,clean and rinse eyes with large amounts of cool tap-water immediately.

Stop Use

Stop use and ask doctor if irritation or rash appears and lasts.

Ask Doctor

Changes in hair color or texture may happen to some persons.

Keep Oot Of Reach Of Children

The amount of hair regrowth is various for each person.This product will not work for all persons.
Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Directions

Use the spray head to apply the serum to the scalp in the area of thinning
Please do an allergy test before use

Other information

Please do an allergy test before use

Inactive ingredients

Water, Butanediol, Phenoxyaethanolum, Hyaluronic acid, VB5, Platycladus orientalis leaf extract, Ginger root extract, Polygonum multiflorum extract

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FYMIOX MINOXIDIL HAIR GROWTH SPRAY. 
minoxidil hair growth spray. spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84213-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BUTANEDIOL (MIXED ISOMERS) (UNII: TMS4MGA0H4)
HYALURONIC ACID (UNII: S270N0TRQY)
GINGER (UNII: C5529G5JPQ)
REYNOUTRIA MULTIFLORA ROOT OIL (UNII: 1HIE915O2J)
PLATYCLADUS ORIENTALIS LEAF (UNII: 32E5V7G32B)
PANTOTHENIC ACID (UNII: 19F5HK2737)
ANISOLE (UNII: B3W693GAZH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84213-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/28/2024
2	NDC: 84213-001-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/28/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	03/28/2024

Labeler - Shenzhen Weilaiwang Technology Co., Ltd (705168691)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Weilaiwang Technology Co., Ltd		705168691	manufacture(84213-001) , label(84213-001)