DIZOP MINOXIDIL TOPICAL GEL- minoxidil 5% gel

Dizop Minoxidil Topical Gel by

Drug Labeling and Warnings

Dizop Minoxidil Topical Gel by is a Otc medication manufactured, distributed, or labeled by Shenzhen Joyuflsh Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Dizop Minoxidil Topical Gel

ACTIVE INGREDIENT

Minoxidil 5%

PURPOSE

Reactivates Hair Follicles To Stimulate RegrowthEasy-To-Use Minoxidil Gel

Minoxidil Topical Gel, 5% (For Men), is designed for men experiencing general hair
thinning on the top of the scalp, as depicted.

INDICATIONS & USAGE

Hair regrowth treatment for men.
Use to Regrow Hair on the Top of the Scalp (See Pictures on the Side of this Carton).

WARNINGS

For external use only

DO NOT USE

Your degree of hair loss differs from that shown on the side of this carton because this product may not work for you.
Your hair loss is sudden, patchy, or a combination of both.
You are under 18 years of age. Please do not use it on babies or children.
Your scalp is red, inflamed, infected, irritated, or painful.
You use other medicines on the scalp.

WHEN USING

Do not use more than directed.
Avoid contact with the eyes, ears, and mouth. In the event of accidental contact withthe eyes, rinse the affected area with a generous amount of cool tap waterimmediately.
lt takes time to regrow hair. Results may occur after two months of once-daily useFor some individuals, it may take at least four months before results becomenoticeable.
The efficacy of this product in promoting hair regrowth can differ from person to person, and it may not work for every man.

STOP USE

Stop use and ask a doctor if you experience chest pain, a rapid heartbeat,faintness, or dizziness, or if scalp irritation or redness occurs. These may be signs of a serious condition

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222

DOSAGE & ADMINISTRATION

Apply 1 ml onto the scalp, where hair loss occurs, once daily and massaging gently for absorption.

STORAGE AND HANDLING

Store between 41 and 86℉ (5 and 30 ℃). Avoid freezing and exposure to excessive heat above 95℉ (35°C)

INACTIVE INGREDIENT

STEARIC ACID
OLEIC ACID
POLYSORBATE 80
SORBITAN MONOOLEATE
CARBOMER HOMOPOLYMER
GLYCERIN
PURIFIED WATER

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DIZOP MINOXIDIL TOPICAL GEL 
minoxidil 5% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83766-101
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
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
STEARIC ACID (UNII: 4ELV7Z65AP)
SORBITAN MONOOLEATE (UNII: 06XEA2VD56)
GLYCERIN (UNII: PDC6A3C0OX)
OLEIC ACID (UNII: 2UMI9U37CP)
WATER (UNII: 059QF0KO0R)
BIOTIN (UNII: 6SO6U10H04)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83766-101-02	1 in 1 CARTON	10/26/2023
1	NDC: 83766-101-01	100 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	10/26/2023

Labeler - Shenzhen Joyuflsh Technology Co.,Ltd. (603012375)

Registrant - Shenzhen Joyuflsh Technology Co.,Ltd. (603012375)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Joyuflsh Technology Co.,Ltd.		603012375	manufacture(83766-101)