HEALMUSZ MINOXIDIL- minoxidil 5%, minoxidil liquid

HEALMUSZ MINOXIDIL by

Drug Labeling and Warnings

HEALMUSZ MINOXIDIL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Minoxidil 5%

Purpose

Hair Regrowth Treatment

Use

to regrow hair on the top of the scalp

Warnings

For external use only
Keep away from fire and flame
Avoid contact with eyes

Do not use

You have no family history of hair loss,hair loss is sudden and/or patchy you are under 18 years of age.Do not use it on babies and children

When Using

Do not apply on other parts of the body
Avoid contact with eyes. In case of accidental contact, rinse eyes with a large amount of cool tap water lt takes time to regrow hair, You may need to use this product 2 timesa day for at least 4 months before you see results, The amount of hair regrowth is different for each person

Stop Use

chest pain, rapid heartbeat, faintness, or dizziness occurs sudden, unexplained weight gain occurs your hands or feet swell scalp irritation or redness occurs

Ask Doctor

chest pain, rapid heartbeat, faintness, or dizziness occurs sudden, unexplained weight gain occurs your hands or feet swell scalp irritation or redness occurs

Keep Oot Of Reach Of Children

lf swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

Directions

Apply half a capful 2 times a day directly to the scalp in the hair loss area Massage into scalp with fingers, then wash well Using more than directed or more often will not improve results.Continued use is necessary to increase and then maintain your hair regrowth

Other information

Before use, read all information on the carton Store at controlled room temperature
20 to 25 C (68 to 77°F)

Inactive ingredients

Deionized Water,Propylene Glycol,Ethyl Alcohol,Potassium Sorbate,GABA

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEALMUSZ MINOXIDIL 
minoxidil 5%, minoxidil liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-041
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)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
.GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-041-01	2 in 1 BOX	10/25/2024
1		50 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	10/25/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-041)