HOQU NAIL FUNGUS SOLUTION- nail fungus solution liquid

Hoqu Nail Fungus Solution by

Drug Labeling and Warnings

Hoqu Nail Fungus Solution by is a Otc medication manufactured, distributed, or labeled by Shenzhen Suai Electronic Science & Technology Co., Ltd., Nanyang Linuo Health Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

chlorhexidine acetate 0.2% v/v

Purpose

bacteriostatic, sterilizing.

Use

Use for fungal nail infections.

Warnings

For external use only

Do not use

It is prohibited for those who are allergic to this product and pregnant women, and should be used with caution on open wounds.

When Using

Do not put in eyes,If it accidentally gets into your eyes, rinse with water or seek medical advice.If irritation or rash occurs, discontinue use and ask a doctor. If swallowed, get medical help or contact a Poison Control Center immediately

Stop Use

Stop use and ask a doctor if irritation or rash occurs.

Ask Doctor

Do not put in eyes,lf it accidentally gets into your eyes, rinse with water or seek medical advice.lf irritation or rash occurs, discontinue use and ask a doctor. if swallowed, get medical help or contact a Poison Control Center immediately

Keep Oot Of Reach Of Children

Please keep this product out of reach of children.

Directions

Apply this product to the desired nail area, 1-2 times a day. Keep using it. Avoid light, airtight, and store in a cool and dry place.

Inactive ingredients

ARTEMISIA ARGYI LVL.ET VAN,ANGELICAE DAHURICAE RADIX,IMPATIENS BALSAMINA L,PHRYMA L,PSEUDOLARIX KAMEPFERI GORD,SOPHORA FLAVESCENS,STEMONASESSILIFOLIA,WATER.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOQU NAIL FUNGUS SOLUTION 
nail fungus solution liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84095-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L)	CHLORHEXIDINE ACETATE	0.2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ)
SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)
3-METHYL-5-HEPTANONE OXIME (UNII: XHN6C9A7U3)
PSEUDOLARIX AMABILIS WHOLE (UNII: G2TMJ38TAU)
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)
IMPATIENS BALSAMINA LEAF (UNII: LH9E1X602V)
PHRYMA LEPTOSTACHYA WHOLE (UNII: 6G287VJM69)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84095-004-01	20 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/09/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	04/09/2024

Labeler - Shenzhen Suai Electronic Science & Technology Co., Ltd. (444420123)

Establishment
Name	Address	ID/FEI	Business Operations
Nanyang Linuo Health Technology Co., Ltd.		619336612	manufacture(84095-004)