Active Ingredient
Minoxidil 5%
Fymiox Minoxidil Hair Growth Spray.
FDA Label NDC 84213-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Weilaiwang Technology Co., Ltd for the product Fymiox Minoxidil Hair Growth Spray. (NDC 84213-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
1 (50ml 00)
2 (60ml 00)
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