84844-016 017

Manufacturer
Guoyu Trading Co., Ltd.
Effective date
2024-11-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:38:17

Label at a glance#

ProductNekvnro Fungal Nail Treatment Kit Fungal Nail Ointment.
Active ingredientTOLNAFTATE
Label structure13 sections

Dosage and administration

■Clean affected areas with soap and warm water and dry thoroughly. ■Apply a thin layer of Nekvnro Anti-Fungal Ointment over affected area twice daily (morning and night) or as directed by a doctor. ■ Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily. ■ For athlete’s foot pay special attention to spaces between the toes. ■For athlete’s foot and ringworm, use daily for 4 weeks. ■To ...

Storage and handling

Store at controlled room temperature 15º-30º C( 59º-86ºF) Protect from freezing.If freezing occurs warm to room temperature.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

30G:

Tolnaftate 1%

50ML:

Tolnaftate 1%

Purpose

OTC - PURPOSE SECTION

Anti-fungal

Use

INDICATIONS & USAGE SECTION

■Proven effective in the treatment of most athlete’s foot (tinea pedis) and ringworm(tinea corporis).
■Helps prevent most athlete's foot with daily use.

■For effective relief of itching, burning and cracking.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on children under 2 years of age unless directed by a doctor.

When Using

OTC - WHEN USING SECTION

this product avoid contact with eyes.

Stop Use

OTC - STOP USE SECTION

and ask a doctor if
■Irritation occurs.

■There is no improvement within 4 weeks.

Ask Doctor

OTC - ASK DOCTOR SECTION

■Irritation occurs.

■There is no improvement within 4 weeks.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a physician, emergency medical care facility or Poison Control Center immediately for advice.

Directions

DOSAGE & ADMINISTRATION SECTION

■Clean affected areas with soap and warm water and dry thoroughly.

■Apply a thin layer of Nekvnro Anti-Fungal Ointment over affected area twice daily (morning and night) or as directed by a doctor.

■ Wear well-fitting, ventilated shoes, and change shoes and socks at least once daily.

■ For athlete’s foot pay special attention to spaces between the toes.

■For athlete’s foot and ringworm, use daily for 4 weeks.

■To prevent athlete's foot, apply once or twice daily(morning and/or night).

■For toe fungus, apply under nail and around cuticle area.If condition persists longer, consult a doctor.

■ This product is not effective on the scalp or nails.

■Supervise children in the use of this product.

Other information

STORAGE AND HANDLING SECTION

Store at controlled room temperature 15º-30º C( 59º-86ºF) Protect from freezing.If freezing occurs warm to room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

30G:

Cetyl alcohol, Glycerin, Monoolein, Salicylic acid,Stearyl alcohol, Urea, Acetic acid,mineral oil,etc.

30ML:

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

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2211

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313423tolnaftate 1 % Topical SolutionPSN1
313423tolnaftate 10 MG/ML Topical SolutionSCD1
313423tolnaftate 1 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84844-016-012026-01-29C16284748780-149896155-a05a-586f-e063-e6dba90add9084844-016 017
84844-017-012026-01-29C16284748780-149896155-a05a-586f-e063-e6dba90add9084844-016 017

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84844-016-01Nekvnro Fungal Nail Treatment Kit Fungal Nail Ointment.30 g in 1 TUBEPASTE301
84844-017-01Nekvnro Fungal Nail Treatment Kit Multi-Purpose Treatment.30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84844-016NEKVNRO FUNGAL NAIL TREATMENT KIT FUNGAL NAIL OINTMENT. (FUNGAL NAIL TREATMENT KIT FUNGAL NAIL OINTMENT.) PASTE NEKVNRO FUNGAL NAIL TREATMENT KIT MULTI-PURPOSE TREATMENT. (FUNGAL NAIL TREATMENT KIT MULTI-PURPOSE TREATMENT.) LIQUID [GUOYU TRADING CO., LTD.]11 package rows20241122_2769f17e-7a38-2d01-e063-6294a90a185f.zip
84844-017NEKVNRO FUNGAL NAIL TREATMENT KIT FUNGAL NAIL OINTMENT. (FUNGAL NAIL TREATMENT KIT FUNGAL NAIL OINTMENT.) PASTE NEKVNRO FUNGAL NAIL TREATMENT KIT MULTI-PURPOSE TREATMENT. (FUNGAL NAIL TREATMENT KIT MULTI-PURPOSE TREATMENT.) LIQUID [GUOYU TRADING CO., LTD.]11 package rows20241122_2769f17e-7a38-2d01-e063-6294a90a185f.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84844-01684844-016-01
84844-01784844-017-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

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
2769f17e-7a39-2d01-e063-6294a90a185f2769f17e-7a38-2d01-e063-6294a90a185f2024-11-21WarningsExact identifier
spl id: 2769f17e-7a39-2d01-e063-6294a90a185f
spl set id: 2769f17e-7a38-2d01-e063-6294a90a185f

Reported adverse events (FAERS/openFDA)#

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