HAIR REGROWTH FOAM aerosol, foam

Hair Regrowth Foam by

Drug Labeling and Warnings

Hair Regrowth Foam by is a Otc medication manufactured, distributed, or labeled by Guangzhou Ariel Biotech Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Minoxidil Sulfate 2%

Purpose

Hair regrowth treatment

Use

Use: To regrow hair of scalp and beard

Warnings

Warnings: For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Keep out of reach of
children.lf you are pregnant, nursing, or have any underlying medical condition, consult your healthcare provider before using
the product.

Do not use

Do not use: on broken or irritated scalp.

WHEN USING

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

STOP USE

●Chest pain, rapid heartbeat, faintness or dizziness occurs.
●Scalp iritation or redness occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

Directions

Directions: Apply 1-2 pumps to palm, rub hands together, and evenly distribute through hair and
directly to scalp in the morning or evening.

Other information

No Data

Inactive ingredients

Inactive ingredients: Allantoin, Aroma, Cocamidopropyl Betaine, Dipropylene Glycol Disodium Cocoamphodiacetate, Disodium Edta,
Ethylhexylglycerin, Glycerin, Panthenol, Phenoxyethano, Sodium Chloride, Sodium Lauroyl Sarcosinate, Water, Xanthan Gum.

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

HAIR REGROWTH FOAM 
hair regrowth foam aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84148-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINOXIDIL SULFATE (UNII: HM46T3593Q) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL SULFATE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
XANTHAN GUM (UNII: TTV12P4NEE)
SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)
PANTHENOL (UNII: WV9CM0O67Z)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
AROMADENDRIN (UNII: 7YA4640575)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84148-006-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/19/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/19/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Ariel Biotech Co., Ltd.		402818771	manufacture(84148-006)