HAIR BEARDGROWTH FOAM- minoxidil liquid

HAIR BEARDGROWTH FOAM by

Drug Labeling and Warnings

HAIR BEARDGROWTH FOAM by is a Otc medication manufactured, distributed, or labeled by Shenzhen Xuemin E-commerce Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

HAIR & BEARDGROWTH FOAM

ACTIVE INGREDIENT

Minoxidil 5%

PURPOSE

Hair regrowth treatment formen

INDICATIONS & USAGE

Use to regrow hairofscalp and beard

WARNINGS

For externaluse only

Keep out ofreach ofchildren.

DO NOT USE

You have no familyhistoryofhair loss

Your hairloss is sudden or patchy.

Your hair loss is associated with childbirth.

You do not know the reason foryourhair loss.

You are under 18 years ofage. Do not use on babies and children.

Your scalp is red, inflamed, infected, or painful.

You use othermedicines on the scalp.

WHEN USING

Avoid contact with eyes. In case ofaccidental contact, rinse eyes with
a large amount ofcool tap water.

STOP USE

If scalp irritation or redness occurs

If you get unwanted facial hair growth.

lf you do not see hairregrowth in 4 months

If sudden unexplained weight gain occurs.

If swallowed, get medical help orcontact a Poison Control Center(1-800-222-1222)right away.

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN SECTION

DOSAGE & ADMINISTRATION

Applya sufficient amount to theclean and dry area ofhair loss,avoiding application to other areas,Gently massage with fingertips for2-3 minutes to facilitate serumabsorption. No rinsing is requiredUse 1-2 times daily. After using thisremember to wash your handsThetotaldailyamount should notexceed2ml. Continued use formonths isnecessary to increaseand thenmaintain your hair regrowth.

INACTIVE INGREDIENT

Biotin

Rosmarinic acid

Castor Oil
Panthenol
Niacinamide
Aloe Vera Extract
Ethanol
Glycerin
Butyleneglycol
Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAIR BEARDGROWTH FOAM 
minoxidil liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85173-001
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
BIOTIN (UNII: 6SO6U10H04)
ROSMARINIC ACID (UNII: MQE6XG29YI)
CASTOR OIL (UNII: D5340Y2I9G)
PANTHENOL (UNII: WV9CM0O67Z)
NIACINAMIDE (UNII: 25X51I8RD4)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ALCOHOL (UNII: 3K9958V90M)
GLYCERIN (UNII: PDC6A3C0OX)
1,3-BUTYLENEGLYCOL DIMETHACRYLATE (UNII: OL56191M6N)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85173-001-01	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/16/2025
2	NDC: 85173-001-02	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/16/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/16/2025

Labeler - Shenzhen Xuemin E-commerce Co., Ltd. (616208436)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Xuemin E-commerce Co., Ltd.		616208436	manufacture(85173-001)