5% MINOXIDIL HAIR REGROWTH FOAM aerosol, foam

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient(s)

5% Minoxidil

Purpose

Hair regrowth treatment

Warnings

For external use only. Avoid contact with eyes.
If contact occurs, rinse thoroughly with water.
Keep out of reach of children.
Discontinue use if any irritation or adverse
reaction occurs.
If you are pregnant, nursing, or have any
underlying medical conditions, consult your
healthcare provider before using the product.

Do not use

Do not use on broken or irritated scalp.

WHEN USING

When using this product, avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Discontinue use if any irritation or adverse reaction occurs.

STOP USE

Discontinue use if any irritation or
adverse reaction occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. This
packaging is designed to prevent child
access.

Other information

store at room temperature

Inactive ingredients

Water, Alcohol Denat, Glycerin,Propylene
Glycol, Potassium Cocoate, Ppg-10 Sorbitol,
Phenoxyethanol, Potassium Cocoyl Hydrolyzed
Oat Protein, Sodium Lauryl Glycol Carboxylate,
Citric Acid, Biota Orientalis Leaf Extract,
Ethylhexylglycerin, Rosmarinus Offcinalis
(Rosemary) Leaf Oil

Use

Use To regrow hair of scalp and beard

Directions

Apply half a capful twice a day to the scalp in
the hair loss area. Massage into the scalp with
fingers, then wash hands well.
Using more or more often will not improve
results. Continued use is necessary to increase
and maintain hair regrowth; otherwise, hair loss
will begin again.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

5% MINOXIDIL HAIR REGROWTH FOAM 
5% minoxidil hair regrowth foam aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84148-025
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 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
SORBITOL (UNII: 506T60A25R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POTASSIUM COCOYL GLUTAMATE (UNII: IR5T90R7LZ)
SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)
CITRIC ACID (UNII: 2968PHW8QP)
PLATYCLADUS ORIENTALIS LEAF (UNII: 32E5V7G32B)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL (UNII: 8LGU7VM393)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84148-025-01	60 g in 1 BOTTLE; Type 0: Not a Combination Product	04/02/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/02/2026

Labeler - Guangzhou Ariel Biotech Co., Ltd. (402818771)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Ariel Biotech Co., Ltd.		402818771	manufacture(84148-025)