MINOXIDIL HAIR REGROWTH TREATMENT- minoxidil liquid

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Minoxidil 5% w/w

Purpose

Hair Regrowth

Use

Use to regrow hair of the scalp and beard growth for men and wemen

Warnings

Warnings
For external use only.
Keep out of reach of children.

Do not use if

Do not use if
You have no family history of hair loss.
Your hair loss is sudden and/or patchy.
Your hair loss is associated with childbirth.
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

When Using
Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water.

Stop Use And Ask A Doctor

Stop Use And Ask A Doctor
Chest pain, rapid heartbeat, faintness, or dizziness occurs.
Sudden, unexplained weight gain occurs.
Scalp irritation or redness occurs.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Keep Out Of Reach Of Children

Keep Out Of Reach Of Children

Directions

Directions
Apply twice a day. Once in the morning and another time in the
evening before bed
Spray directly on top of the scalp in the area to be treated
Using more than directed or more often will not improve results
Continued use is necessary to lncrease and then malntain your
hair regrowth

Other information

Other information
Before use, read all information on carton and enclosed leaflet.
Store at controlled room temperature 10° to 30°C (50° to 80°F).
Do not incinerate container. Do not expose to heat or store at temperature above 104°F (40°C).

Inactive ingredients

Water, Propylene Glycol, Potassium Sorbate, Castor Oil, Lavender Oil, Cymbopogon Citratus Leaf, Chamomile, Biotin , Rosemary Oil, Ginger, Batana Oil

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MINOXIDIL HAIR REGROWTH TREATMENT 
minoxidil liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85636-024
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
CASTOR OIL (UNII: D5340Y2I9G)
WATER (UNII: 059QF0KO0R)
CHAMOMILE (UNII: FGL3685T2X)
CYMBOPOGON CITRATUS LEAF (UNII: 06JMS448M5)
ROSEMARY (UNII: IJ67X351P9)
BIOTIN (UNII: 6SO6U10H04)
LAVENDER OIL (UNII: ZBP1YXW0H8)
GINGER (UNII: C5529G5JPQ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85636-024-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	05/01/2026

Labeler - Shenzhen Earth Surface Trading Co., Ltd. (454290055)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Earth Surface Trading Co., Ltd.		454290055	manufacture(85636-024) , label(85636-024)