Fungal Nail Patches

Manufacturer
GUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD | Guangzhou Meixi Biotechnology Co., Ltd.
Effective date
2025-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:15:06

Label at a glance#

ProductFungal Nail Patches
Active ingredientTOLNAFTATE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

TOLNAFTATE 1%

OTC - PURPOSE SECTION

Antifungal

INDICATIONS & USAGE SECTION

For the effective treatment of nall fungus, discoloration, thickening, splitting, crumbling and brittleness.
Restore and improve the appearance of nails that have been affected by fungus.

WARNINGS SECTION

For external use only. Store in a cool place and avoid sunshine and heat.

OTC - DO NOT USE SECTION

Do not use · on children under 2 years of age unless directed by a doctor.

OTC - WHEN USING SECTION

When using this product · avoid contact with the eyes or damaged skin.It's normal to feel a slight, temporary sensation of irritation, tingling, or burning. lf symptoms persist or worsen,discontinue use.

OTC - STOP USE SECTION

Stop use and ask a doctor if . irritation occurs or if there is no improvement within 4 weeks.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

1.Clean and dry the affected nail and surrounding area.
2.Remove the patch from its protective film.
3.Place it directly onto the infected nail, ensuring full coverage.
4. Gently press down on the edges of the patch to make sure it is firmly adhered to the nail and skin, with no airbubbles.
5. Keep the patch on for 24 hours. Replace it once a day, preferably after showering.

INACTIVE INGREDIENT SECTION

WATER
UREA
LACTIC ACID
GLYCERIN
TERPINEN-4-OL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2677690tolnaftate 1 % Medicated PatchPSN1
2677690tolnaftate 0.01 MG/MG Medicated PatchSCD1
2677690tolnaftate 1 % Medicated PatchSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85966-006-01Fungal Nail Patches1 in 1 PATCHPATCH11
85966-006-01Fungal Nail Patches32 in 1 BOXPATCH321

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85966-00685966-006-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
Fungal Nail PatchesTOLNAFTATEGUANGZHOU SAWEILAN IMPORT & EXPORT TRADING CO., LTD3fe861cc-c972-a328-e063-6294a90afc8f2025-09-28WarningsExact identifier
ndc (package): 85966-006-01
ndc (product): 85966-006
ndc11 (package): 85966000601
spl id: 3fe861cc-c973-a328-e063-6294a90afc8f
spl set id: 3fe861cc-c972-a328-e063-6294a90afc8f

Reported adverse events (FAERS/openFDA)#

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