84558-031

Manufacturer
GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd
Effective date
2026-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-22 01:01:46

Label at a glance#

Product5% MINOXIDIL SERUM
Active ingredientMINOXIDIL
Label structure12 sections

Dosage and administration

Apply 1 mL twice a day directly onto the scalp in the hair loss area for men only. Using more or more often will not improve results. Loss will begin again if use is stopped. Continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again.

Storage and handling

Store at 20-25°C (68-77°F). Keep tightly closed. Before use, read all information on carton. Keep the carton. It contains important information.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5% w/v

Purpose

OTC - PURPOSE SECTION

Hair Regrowth Treatment

Use

INDICATIONS & USAGE SECTION

Use to regrow hair on the vertex (top of
scalp) in men with androgenetic alopecia.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

▪ you are a woman
▪ your hair loss pattern is different from the examples shown on the carton
▪ you have no family history of hair loss
▪ your hair loss is sudden and/or patchy
▪ you do not know the reason for your hair loss
▪ you are under 18 years of age
▪ your scalp is red, inflamed, infected, irritated, or painful
▪ you use other medicines on the scalp

Ask a doctor before use if you have heart disease.

OTC - WHEN USING SECTION

▪ do not apply on other parts of the body
▪ avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water.
▪ some people have experienced changes in hair color and/or texture
▪ it takes time to regrow hair. Results may occur at 2 months with twice a day usage. For some people, you may
need to use this product for at least 4 months before you see results.
▪ the amount of hair regrowth is different for each person.

This product will not work for all people.

OTC - STOP USE SECTION

▪ chest pain, rapid heartbeat, faintness, or dizziness occurs
▪ sudden, unexplained weight gain occurs
▪ your hands or feet swell
▪ scalp irritation or redness occurs
▪ unwanted facial hair growth occurs
▪ you do not see hair regrowth in 4 months
▪ If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away at
1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply 1 mL twice a day directly onto the
scalp in the hair loss area for men only.
Using more or more often will not improve
results. Loss will begin again if use is
stopped. Continued use is necessary to
increase and keep your hair regrowth, or
hair loss will begin again.

Other information

STORAGE AND HANDLING SECTION

Store at 20-25°C (68-77°F). Keep tightly closed.
Before use, read all information on carton. Keep the carton. It contains important information.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin,
Butanediol, Glycine, Xanthan Gum,
PEG-40 Hydrogenated Castor Oil.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84558-03184558-031-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5% MINOXIDIL SERUM5% MINOXIDIL SERUMGUANGZHOU YUSONG FINE CHEMICLS Co., Ltd595d2e2f-ce05-3a42-e063-6294a90ab0d22026-08-18WarningsExact identifier
ndc (package): 84558-031-01
ndc (product): 84558-031
ndc11 (package): 84558003101
spl id: 595d2fa4-5108-3867-e063-6294a90ae1e4
spl set id: 595d2e2f-ce05-3a42-e063-6294a90ab0d2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.