LILIVERA HAIR REGROWTH KIT- minoxidil liquid

LILIVERA Hair Regrowth Kit by

Drug Labeling and Warnings

LILIVERA Hair Regrowth Kit by is a Otc medication manufactured, distributed, or labeled by Guangzhou Haishi Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Minoxidil 5%

Purpose

Hair regrowth treatment

Uses

lt only works with the vertex, not with the forehead or temporal alopecia.

Don't drop more than 4 times each time because your scalp wouldn't absorb it.

Warnings

For external use only.

Stop use and ask a doctor if

rash occurs.

Do not use

Pregnant, breastfeeding, under 18, have heart issues, super-sensitive skin,open wounds, or after using a derma roller (may cause irritation).
Missing the sulfate transferase enzyme (minoxidil will not be effective).
Suffering hair loss for over 5 years, or targeting hairline/temple baldness(only works on the vertex).

When using this product

Avoid contact with eyes. If accidentally in contact with the eyes, please rinse the eyes with plenty of cold water.

Keep out of reach of children.

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

Dosage

Don't drop more than 4 times each time because your scalp wouldn't absorb it.

Inactive ingredients

WATER 59.425%
GLYCERIN 5%
BUTYLENE GLYCOL 5%
PANTHENOL 1%
TRIPEPTIDE-1 2%
AZELAIC ACID 2%
NIACINAMIDE 2%
MENTHA ARVENSIS LEAF EXTRACT 0.83%
HYDRANGEA MACROPHYLLA LEAF EXTRACT 0.83%
ALOE BARBADENSIS LEAF EXTRACT 0.83%
PORTULACA OLERACEA EXTRACT 0.83%
CHRYSANTHELLUM INDICUM EXTRACT 0.83%
SOPHORA ANGUSTIFOLIA ROOT EXTRACT 0.85%
CENTELLA ASIATICA ROOT EXTRACT 2%
ALCOHOL 3%
CURCUMIN 0.5%
HYDROLYZED WHEAT PROTEIN 2%
MOROCCAN NUT OIL 2%
ROSA CANINA FRUIT OIL 1%
SODIUM HYALURONATE 1%
BIOTIN 1%
RETINOL 0.025%
HYDROXYACETOPHENONE 0.5%
1,2-HEXANEDIOL 0.5%
DISODIUM EDTA 0.05%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LILIVERA HAIR REGROWTH KIT 
minoxidil liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0012
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
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PANTHENOL (UNII: WV9CM0O67Z)
TRIPEPTIDE-1 (UNII: 39TG2H631E)
MENTHA ARVENSIS LEAF (UNII: A4IWO4DDZ9)
GLYCERIN (UNII: PDC6A3C0OX)
NIACINAMIDE (UNII: 25X51I8RD4)
AZELAIC ACID (UNII: F2VW3D43YT)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0012-1	60 mL in 1 BOTTLE, DROPPER; Type 1: Convenience Kit of Co-Package	04/18/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	04/18/2025

Labeler - Guangzhou Haishi Biological Technology Co., Ltd. (421262738)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		421262738	manufacture(60771-0012)