XAFVRQ HAIR REGROWTH TREATMENT- minoxidil wiht biotin 5% liquid

XAFVRQ Hair Regrowth Treatment by

Drug Labeling and Warnings

XAFVRQ Hair Regrowth Treatment by is a Otc medication manufactured, distributed, or labeled by COMART TECH LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

5%minoxidil wiht Biotin

PURPOSE

Hair Regrowth

INDICATIONS & USAGE

1. Massage the scalp to fully relax the scalp.

2. Ad one or two drops to the scalp area to be used.

3. Apply evenly to the rest of the area.

4. Continue to use weice a day.

WARNINGS

For external use only.For external use only
Keep away from fire and flame

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

WHEN USING

1. Do not apply on other parts of the body, For topical use only on the scalp.

2. Avoid contact with the eyes in case of accidental contact rinse eyes with large arnounts of cool tap water.

3. Some people have experienced changes in hair color and/or texture.

4. The amount of hair regrowth is dlfferent for each person. This product will not work for all men.

Usage:1. Massage the scalp to fully relax the scalp.2. Ad one or two dropsto the scalp area to be used.3. Apply evenly to the rest of the area.4. Continue to use weice a day.

Friendly reminder: it takes time to regrow hair, it usually takes 45-60 days to see the effect, the speciflc effect will vary from person to person, some people may need 90 days to see the effect.

DO NOT USE

You have no family history of hair loss,hair loss is sudden and/or patchy.
You do not know the reason for you hair loss.
You ae under 18 years of age, Do not use it on babies and children your scalp is red,inflamed,infected, irritated, or painful.
You use other medicines on the scalp.Ask a doctor before use if you hace heart disease.

STOP USE

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

INACTIVE INGREDIENT

INGREDIENTS:
Water, Butanediol, Rosenmary, Hyaluronic Acid, VB5,Platycladus Orientalis Leaf Extract, Ginger Root Extract, Polygonum Multiflorum Extract, TobaccoExtract, Lemon Extract, Sweet Orange Extract.Caffeine, Turmeric Extract, Vigna Radiata,Red Clover, Phenoxyaethanolum

DOSAGE & ADMINISTRATION

Twice each day, 4 sprays (1ml)each time. 50 days supply

PRINCIPAL DISPLAY PANEL

INGREDIENTS:
Water, Butylene Glycol, Rosmarinus Officinalis (rosemary) Extract, Hyaluronic Acid, VB5,Platycladus Orientalis Leaf Extract, Ginger RootExtract, Polygonum Multiflorum Extract, TobaccoExtract, Lemon Extract, Sweet Orange Extract,Caffeine, Turmeric Extract, Vigna Radiata,Red Clover, Phenoxyaethanolum

FRIENDLY REMINDE

1.Please spray on your scalp, not your hair.2.lt is best not to wash your hair within 2 hours afterspraying so that the medicine can be fully absorbed

3.lt takes time to regrow hair, it usually takes 45-60days to see the effect, the specific effect will vary fromperson to person, some people may need 90 days tosee the effect.

4.You may notice increased hair loss in the first 2-4weeks of the treatment. That is normal since the bodyis getting rid of the dead hair shafts to make room fornew healthy ones

INGREDIENTS AND APPEARANCE

XAFVRQ HAIR REGROWTH TREATMENT 
minoxidil wiht biotin 5% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84542-259
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MINOXIDIL (UNII: 5965120SH1) (MINOXIDIL - UNII:5965120SH1)	MINOXIDIL	5 g  in 60 mL
BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04)	BIOTIN	5 g  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PANTOTHENIC ACID (UNII: 19F5HK2737)
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HYALURONIC ACID (UNII: S270N0TRQY)
CAFFEINE (UNII: 3G6A5W338E)

Product Characteristics
Color		Score
Shape	ROUND	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84542-259-01	120 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/02/2025	01/02/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/02/2025	01/02/2026

Labeler - COMART TECH LLC (131800982)