FDA.reportPublic FDA data

HOQU Nail fungus cream

Manufacturer
Shenzhen Suai Electronic Science & Technology Co., Ltd.
Effective date
2024-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:08:56

Label at a glance#

ProductHOQU Nail fungus cream
Active ingredientCHLORHEXIDINE ACETATE
Label structure12 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

chlorhexidine acetate 0.35%

Purpose

OTC - PURPOSE SECTION

bacteriostatic, sterilizing

Use

INDICATIONS & USAGE SECTION

Use for fungal nail infections

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

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

When Using

OTC - WHEN USING SECTION

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. lf swallowed, get medical help or contact a Poison Control Center immediately

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs

Ask Doctor

OTC - ASK DOCTOR SECTION

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

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep this product out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

Borneol,CORTEX DICTAMNI, cnidium monnieri(L)cuss, camphor,Cortex Phellodendri chinensis, lanolin,Pseudolarix kamepferi Gord，Sophorae Flavescentis Radix, white vaseline, water.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122334455667788

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84095-00284095-002-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLORHEXIDINE ACETATE5908ZUF22YACTIB
DICTAMNUS DASYCARPUS ROOT6153LEN214IACT
CAMPHORIC ACID, (-)-62F72U898FIACT
WHITE PETROLATUMB6E5W8RQJ4IACT
QUERCUS SUBER BARK8R5219271QIACT
WATER059QF0KO0RIACT
BORNEOLM89NIB437XIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
LANOLIN7EV65EAW6HIACT
PSEUDOLARIX AMABILIS BARK49G13A93VEIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
13eb9a4a-deed-5677-e063-6394a90a1cc6135fe874-2970-68a1-e063-6294a90aa2982024-03-18WarningsExact identifier
spl set id: 135fe874-2970-68a1-e063-6294a90aa298

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.