Otc - Active Ingredient
Minoxidil
Gze 5% Minoxidil Solution
FDA Label NDC 74458-270
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Yilong Cosmetics Co., Ltd for the product Gze 5% Minoxidil Solution (NDC 74458-270). 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 otc - active ingredient, inactive ingredient, indications & usage, otc - purpose, warnings, otc - stop use, otc - do not use, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Aqua, Propylene Glycol
Indications & Usage
Apply one mL with spray 2X a day directly onto scalp in the needed area.
Otc - Purpose
Hair growth.
Warnings
For external use only.
Otc - Stop Use
Stop use and ask a doctor if rash occurs.
Otc - Do Not Use
Do not use on damaged or broken skin.
Otc - When Using
When using this product keep out of eyes. Rinse with water to remove.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Apply one mL with spray 2X a day directly onto scalp in the needed area.
Package Label.Principal Display Panel
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