Nincrane 5% Minoxidil for Men

Manufacturer
Clearchic, Inc.
Effective date
2023-10-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:22:47

Label at a glance#

ProductNincrane 5% Minoxidil for Men
Active ingredientMINOXIDIL
Label structure14 sections

Dosage and administration

• Apply one mL with dropper 2 times a day directly onto the scalp in the hair loss area. • 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

• See hair loss pictures on side of this carton. • Before use, read all information on carton and enclosed leaflet. • Keep this carton, It contains important information. • Clinical research in mostly white men aged 18-49 years with moderate degrees of hair loss, showed that minoxidil topical solution 5% proves more hair regrowth than minoxidil topical solution 2% for men. • Store at controlled room temperature be...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

Purpose

OTC - PURPOSE SECTION

Hair regrowth treatment for men

Use

INDICATIONS & USAGE SECTION

to regrow hair on the top of the scalp (vertex only, see pictures on side of the carton)

Warnings

WARNINGS SECTION

For external use only.
Flammable: Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

• You are a woman. • Your level of hair loss is different from that shown on the side of this carton, or your hair loss is on the front of the scalp. Hair Regrowth Treatment 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.

When Using

OTC - WHEN USING SECTION

1. Do not apply on other parts of the body. For topical use only on the scalp.
2. Avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water.
3. Some people have experienced changes in hair color and/or texture.
4. The amount of hair regrowth is different for each person. This product will not work for all men.

Stop Use

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.

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have a heart disease

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

May be harmful if used when pregnant or breast-feeding.Keep out of reach of children. If swallowed, get medical help or contact
Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply one mL with dropper 2 times a day directly onto the scalp in the hair loss area.
• 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.

Other information

STORAGE AND HANDLING SECTION

• See hair loss pictures on side of this carton.

• Before use, read all information on carton and enclosed leaflet.

• Keep this carton, It contains important information.

• Clinical research in mostly white men aged 18-49 years with moderate degrees of hair loss, showed that minoxidil topical solution 5% proves more hair regrowth than minoxidil topical solution 2% for men.

• Store at controlled room temperature between 68°-77°F (2°0-25°C). Keep tightly closed

Inactive ingredients

INACTIVE INGREDIENT SECTION

alcohol, propylene glycol, purified water

Questions

OTC - QUESTIONS SECTION

support@clearchicinc.com

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

0101

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83770-001-012024-01-30C16284748780-11030e365-62b5-111a-e063-dadaa90a10e208ffb0af-a62f-57fe-e063-6294a90a067e

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83770-00183770-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
28f560c7-43e5-3ebb-e063-6394a90ab5b808ffb0af-a62f-57fe-e063-6294a90a067e2024-12-10WarningsExact identifier
spl set id: 08ffb0af-a62f-57fe-e063-6294a90a067e

Reported adverse events (FAERS/openFDA)#

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