87986-001 5% Minoxidil Foam
- Manufacturer
- HONG KONG YUEJIE INTERNATIONAL TRADING LIMITED
- Effective date
- 2026-09-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-09-04 01:01:10
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Minoxidil 5%
OTC - PURPOSE SECTION
For female hair regrowth
INDICATIONS & USAGE SECTION
Helps regrow hair on the scalp
WARNINGS SECTION
For external use only
Flammable: Keep away from fire or flames
OTC - DO NOT USE SECTION
You are experiencing sudden hair loss or patchy hair loss
You do not know the cause of hair loss
You are under 18 years old. This product is not for infants and children
You are taking other medications on your scalp
You have scalp irritation including redness, inflammation, pain, or bacterial infection
OTC - WHEN USING SECTION
Ask a doctor before use if you have heart disease
Do not exceed the recommended dosage and do not use on other parts of the body except the scalp
Avoid contact with eyes. If eye contact occurs, rinse thoroughly with plenty of cool water
Hair color or hair texture may change during use
Hair regrowth takes time, and resultsvary among individuals over 3-6 months of use.
Apply once daily. Consistent use over several months is required to see results.
Responses to treatment vary, so this product may not work for all women.
OTC - STOP USE SECTION
Chest pain, rapid heartbeat, dizziness
Sudden weight gain occurs
Swelling of hands or feet
Abnormal scalp irritation and redness of the scalp
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
May be harmful if used when
pregnant or breast-feeding. Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Avoid children's contact with minoxidil-treated application sites.
Skin contact by children with a caregiver's minoxidil-treated skin may result in hypertrichosis (excessive hair growth).
DOSAGE & ADMINISTRATION SECTION
Press out half a capful of foam once daily and apply it evenly to the area of the scalp (not hair) where hair regrowth is desired
Massage in with fingers; wash hands after
More frequent use will not improve results
Continued use is needed to maintain regrowth
INACTIVE INGREDIENT SECTION
GLYCERIN
CETYL ALCOHOL
STEARYL ALCOHOL
SODIUM LAUROYL SARCOSINATE
WATER
POLYSORBATE 80
ANHYDROUS CITRIC ACID
LACTIC ACID, UNSPECIFIED FORM
CASTOR OIL
.ALPHA.-TOCOPHEROL
EDETATE SODIUM
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
label
Products#
Every source-derived product name is available through these pages.
- 5% Minoxidil Foam
- Minoxidil
- GLYCERIN
- CETYL ALCOHOL
- STEARYL ALCOHOL
- SODIUM LAUROYL SARCOSINATE
- WATER
- POLYSORBATE 80
- ANHYDROUS CITRIC ACID
- LACTIC ACID, UNSPECIFIED FORM
- CASTOR OIL
- .ALPHA.-TOCOPHEROL
- EDETATE SODIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 87986-001 | 87986-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MINOXIDIL | 5965120SH1 | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| CETYL ALCOHOL | 936JST6JCN | IACT |
| STEARYL ALCOHOL | 2KR89I4H1Y | IACT |
| SODIUM LAUROYL SARCOSINATE | 632GS99618 | IACT |
| WATER | 059QF0KO0R | IACT |
| POLYSORBATE 80 | 6OZP39ZG8H | IACT |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| LACTIC ACID, UNSPECIFIED FORM | 33X04XA5AT | IACT |
| CASTOR OIL | D5340Y2I9G | IACT |
| .ALPHA.-TOCOPHEROL | H4N855PNZ1 | IACT |
| EDETATE SODIUM | MP1J8420LU | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 5% Minoxidil Foam | MINOXIDIL | HONG KONG YUEJIE INTERNATIONAL TRADING LIMITED | 5a7b2dec-4879-7491-e063-6394a90a874f | 2026-09-02 | Warnings | 87986-001-01 87986-001 87986000101 5a7b2dec-487a-7491-e063-6394a90a874f 5a7b2dec-4879-7491-e063-6394a90a874f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
