Other
RUIGOO MINOXIDIL TOPICAL GEL
Ruigoo Minoxidil Topical Gel
FDA Label NDC 83767-101
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 Ruijiu Electronic Technology Co., Ltd. for the product Ruigoo Minoxidil Topical Gel (NDC 83767-101). 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 other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
MINOXIDIL 5%
Otc - Purpose
Hair regrowth treatment for women.
Use to regrow hair on the top of the scalp.
Indications & Usage
is for Women who have a general thinning of hair onthe top of the scalp as shown.
Warnings
For external use only.
Otc - Do Not Use
Your degree of hair loss is different than that shown on side of this cartonbecause this product may not work for you.
Your hair loss is sudden and/or patchy
You are under 18 years of age. Do not use on babies or children
Your scalp is red, inflamed, infected, irritated, or painful
You use other medicines on the scalp
Otc - When Using
Do not use more than directed.
Avoid contact with the eyes, ears, and mouth. In case of accidental contact, rinse eyes with large amounts of cool tap water.
lt takes time to regrow hair. Results may occur at 2 months with once dailyuse. For some individuals, it may take at least 4 months before resultsbecome noticeable.
The amount of hair regrowth is different for each person. This product will not work for all women.
Otc - Stop Use
Stop use and ask a doctor if you experience chest pain, rapidheartbeat, faintness, or dizziness occurs, Scalp irritation or redness occurs.These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. lf swallowed, get medical help orcontact a Poison Control Center right away.(1-800-222-1222)
Dosage & Administration
Apply 1ml once daily, gently massaging to enhance absorption.
Storage And Handling
Store between 41-86 ℉ (5-30 ℃). Avoid freezing and exposure to excessiveheat above 104 ℉ (40 ℃)
Inactive Ingredient
STEARIC ACID
OLEIC ACID
POLYSORBATE 80
SORBITAN MONOOLEATE
CARBOMER HOMOPOLYMER
CETYL ALCOHOL
CITRIC ACID MONOHYDRATE
GLYCERIN
PURIFIED WATER
Package Label.Principal Display Panel
Label (Label)
* Please review the disclaimer below.
