Elevate 5% Minoxidil Liquid

Manufacturer
Foshan Yilai Cosmetics Co., Ltd.
Effective date
2024-01-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:13:48

Label at a glance#

ProductElevate 5% Minoxidil Liquid
Active ingredientMINOXIDIL
Label structure12 sections

Storage and handling

store at 20"to 25"(68 to 77F). Keep tightly closed.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Minoxidil 5%

OTC - PURPOSE SECTION

Hair regrowth treatment

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. (1-800-222-1222)

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
you do not see hair regrowth in 4 months

WARNINGS SECTION

May be harmful if used when pregnant or breast-feeding.

For external use only. For use on scalp only.
Avoid contact with eyes.

INACTIVE INGREDIENT SECTION

Propylene Glycol, Alcohol, Aqua, Panax Ginseng Extract, Panthenol (Pro-Vitamin B5)

DOSAGE & ADMINISTRATION SECTION

Spray 1ml (5 sprays) twice a day. Once in the morning and another time in the evening before bed. Use only on fully dry hair. Spray directly on top of the scalp of hair loss area. Results can vary and take time but we recommend at least 3-5 months of usage.

STORAGE AND HANDLING SECTION

store at 20"to 25"(68 to 77F). Keep tightly closed.

INDICATIONS & USAGE SECTION

-Prevent and Stop Hair Loss
-Stimulate Hair Growth
-Improve Fullness of Hair
-Restore Vitality of Hair
-Strengthen and Activate Hair Follicles

DESCRIPTION SECTION

Elevate 5% Minoxidil
is applied to the scalp and used to stimulate hair growth in adult men and women. It’s a spray solution that’s been approved by the FDA to treat hair loss and help regrow hair.

ALARMS

Minoxidil may cause side effects. Discontinue use
immediately or tell your doctor if any of these symptoms
are severe or do not go away: scalp itching, dryness,
scaling, flaking, irritation, or burning.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Elevate 5% Minoxidil LiquidElevate 5% Minoxidil Liquid

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83830-10183830-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
130e6d44-96d6-6af0-e063-6294a90a5a6c07044e58-c9cf-3161-e063-6394a90ae0ba2024-03-07WarningsExact identifier
spl set id: 07044e58-c9cf-3161-e063-6394a90ae0ba

Reported adverse events (FAERS/openFDA)#

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