XEXLVOV HELPS WITH NAGELPILZ

Manufacturer
Shanghai Honghui Chuang Intelligent Technology Co., Ltd
Effective date
2026-07-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-07-25 05:10:21

Label at a glance#

ProductHELPS WITH NAGELPILZ
Active ingredientTOLNAFTATE
Label structure12 sections

Dosage and administration

For athlete's foot and ringworm:use daily for 4 weeks.Clean the affected area and dry thoroughly.Keep away from fire and flames.For external use on nails and the immediately adjacent skin only.Use once daily, preferably before bedtime. Unscrew the bottle cap and use the brush to apply the medicine directly to the nail.The medication will then penetrate deeply into the nail.If the nail area is infected,spray the me...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Tolnaftate 1%

Purpose

INDICATIONS & USAGE SECTION

Antifungal

Use

OTC - PURPOSE SECTION

Antifungal treatment for fingernails,toenails, and surrounding skin.Effective against fungal nails and athlete's foot caused by fungi.

Warnings

DOSAGE & ADMINISTRATION SECTION

For external use only.

Do not use

WARNINGS SECTION

if you experience any signs of sensitivity or irritation

When Using

OTC - WHEN USING SECTION

Not for use in the eyes, mouth,or vaginal area.

Stop Use

OTC - STOP USE SECTION

If the area of application shows increased irritation

If there is Consult a doctor if symptoms worsen.

If pregnant or breastfeeding

Ask Doctor

OTC - ASK DOCTOR SECTION

If the area of application shows increased irritation
If there is Consult a doctor if symptoms worsen.
If pregnant or breastfeeding

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If accidental ingestion occurs,seek medical assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

For athlete's foot and ringworm:use daily for 4 weeks.Clean the affected area and dry thoroughly.Keep away from fire and flames.For external use on nails and the immediately adjacent skin only.Use once daily, preferably before bedtime.

Unscrew the bottle cap and use the brush to apply the medicine directly to the nail.The medication will then penetrate deeply into the nail.If the nail area is infected,spray the medication onto the affected area.
SHAKE WELL BEFORE USE.
Store at 5°C to 30°C(41°F to 86°F) in a cool dry place.
Keep tightly closed and away from sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water,euphorbia hirta whole, glycerin,hydracrylic acid, pseudolarix amabilis bark, resorcinol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HELPS WITH NAGELPILZHELPS WITH NAGELPILZ

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136979843982122GTIN-13: 6979843982122
EAN-13: 6979843982122
GTIN storage (14 digits): 06979843982122
f6bf895414644e3ab13b78e360b94a8d.jpg

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87312-11587312-115-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-06-30weekly-update2026-07-17 21:41:43

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
HELPS WITH NAGELPILZTOLNAFTATE 1% HELPS WITH NAGELPILZ LIQUIDShanghai Honghui Chuang Intelligent Technology Co., Ltd55753a4a-a4d0-a183-e063-6394a90acf112026-07-22WarningsExact identifier
ndc (package): 87312-115-01
ndc (product): 87312-115
ndc11 (package): 87312011501
spl id: 5731145d-3b00-8f6d-e063-6294a90a05e5
spl set id: 55753a4a-a4d0-a183-e063-6394a90acf11

Reported adverse events (FAERS/openFDA)#

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