Active Ingredient

Manufacturer
Guangzhou Jingliang Cosmetics Co., Ltd.
Effective date
2026-09-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-08 02:01:53

Label at a glance#

ProductFIGTORUS Minoxidil Hair Growth Treatment
Active ingredientMINOXIDIL
Label structure12 sections

Indications and uses

- to regrow hair on the top of the scalp (vertex only) and promote beard growth on the face

Dosage and administration

- apply 3-4 pumps of foam directly to the treated area of the scalp - after massaging the scalp with your fingertips, wash your hands thoroughly - 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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

Ask a doctore before use

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have heart disease

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Purpose

OTC - PURPOSE SECTION

Hair regrowth treatment

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if

- 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

When Using

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. You may need to use this product twice a day

for at least 4 months

- the amount of hair regrowth is different for each person. This product will

not work for everyone

Inactive ingredients

INACTIVE INGREDIENT SECTION

Biotin, alcohol, propylene glycol, purified water

Directions

DOSAGE & ADMINISTRATION SECTION

- apply 3-4 pumps of foam directly to the treated area of the scalp

- after massaging the scalp with your fingertips, wash your hands thoroughly

- 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

Warnings

WARNINGS SECTION

For external use only.

Uses

INDICATIONS & USAGE SECTION

- to regrow hair on the top of the scalp (vertex only) and promote beard growth on the face

Do Not Use

OTC - DO NOT USE SECTION

- you have no family history of hair loss

- your hair loss is sudden and/or patchy

- your hair loss is due to other causes, such as thyroid disease,

chemotherapy, or scarring

- 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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Brand: FIGTORUS

Name:
FIGTORUS Minoxidil Hair Growth Tretament

Size: 60g x 3 Bottles

package designpackage design

Products#

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DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87408-03387408-033-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
FIGTORUS Minoxidil Hair Growth TreatmentMINOXIDIL HAIR GROWTH TREATMENTGuangzhou Jingliang Cosmetics Co., Ltd.5aa2da98-9015-1a91-e063-6394a90ad7ff2026-09-03WarningsExact identifier
ndc (package): 87408-033-01
ndc (product): 87408-033
ndc11 (package): 87408003301
spl id: 5aa2db1d-dda9-b0d7-e063-6294a90a67a5
spl set id: 5aa2da98-9015-1a91-e063-6394a90ad7ff

Reported adverse events (FAERS/openFDA)#

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