Hair Regen - Hair Regrowth Treatment

Manufacturer
Yiwu Yizhou Trading Co., Ltd
Effective date
2025-04-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:39:53

Label at a glance#

ProductHair Regen - Hair Regrowth Treatment
Active ingredientMINOXIDIL
Label structure13 sections

Dosage and administration

see enclosed booklet for complete directions. apply half a capful once daily directly to the scalp in the hair loss area. massage into scalp with fingers, then wash hands well. using more or more often will not improve results. continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again.

Storage and handling

Store at controlled room temperature 68-77℉ (20-25℃). Contents under pressure. Do not puncture or incinerate container. Do not expose to heat or store at temperaures above 120℉ (49℃).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5% w/w (without propellant)

Purpose

OTC - PURPOSE SECTION

Hair regrowth treatment

Use

INDICATIONS & USAGE SECTION

for women who have general thinning of hair on top of the scalp (vertex only, as shown below).

Warnings

WARNINGS SECTION

For external use only. For use by men only.

Extremely Flammable: Avoid fire, flame, or smoking during and immediately following application.

Do not use if

OTC - DO NOT USE SECTION

  • your amount of hair loss is different than that shown on the side of this carton or your hair loss is on the front of the scalp. 5% minoxidil topical foam is not intended for frontal baldness or receding hairline.
  • 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. Do not use on babies and children.
  • your scalp is red, inflamed, infected, irritated, or painful.
  • you use other medicines on the scalp.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have heart disease

When using this product

OTC - WHEN USING SECTION

  • do not use more than directed.
  • 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.
  • results may occur at three months with consistent daily use. For some women, you may need to use this product once a day for at least six months before you see results.
  • the amount of hair regrowth is different for each person. This product will not work for all women.

Stop use and ask a doctor if ...

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.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical helf or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • see enclosed booklet for complete directions.
  • apply half a capful once daily directly to the scalp in the hair loss area.
  • massage into scalp with fingers, then wash hands well.
  • using more or more often will not improve results.
  • continued use is necessary to increase and keep your hair regrowth, or hair loss will begin again.

STORAGE AND HANDLING SECTION

Store at controlled room temperature 68-77℉ (20-25℃).

Contents under pressure. Do not puncture or incinerate container. Do not expose to heat or store at temperaures above 120℉ (49℃).

Inactive ingredients

INACTIVE INGREDIENT SECTION

butane, butylated hydroxytoluene, cetyl alcohol, citric acid, glycerin, isobutane, lactic acid, polysorbate 60, propane, purified water, SD alcohol 40-B, stearyl alcohol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

W19:

W19W19

W-01:

0101

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84232-01984232-019-01, 84232-019-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
32baa601-248e-0781-e063-6294a90ae3753247dd02-efaf-e176-e063-6294a90ae7392025-04-14WarningsExact identifier
spl set id: 3247dd02-efaf-e176-e063-6294a90ae739

Reported adverse events (FAERS/openFDA)#

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