FDA.reportPublic FDA data

84763-017 FUNGAL NAIL PATCHES

Manufacturer
Yunqi Cosmetics (Shenzhen) Co., Ltd
Effective date
2026-08-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-19 00:01:52

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

Helps improve the appearance of discolored, damaged nails caused by fungal exposure.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

On children under 2 years of age unless directed by a doctor If you are allergic to any ingredient in this product

OTC - WHEN USING SECTION


Avoid contact with eyes
Do not use on broken or severely damaged skin
Discontinue use if irritation or redness develops

OTC - STOP USE SECTION

Irritation worsens
There is no improvement within 4 weeks
Symptoms recur after improvement

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

1. Wash and dry the affected nail thoroughly.
2. Apply one patch to the affected nail before bedtime.
3. Leave the patch on for at least 10 hours or overnight.
4. Remove the patch in the morning and discard after use.
5. Repeat nightly or as directed.

INACTIVE INGREDIENT SECTION

Acrylic Adhesive
Ethylene/Vinyl Acetate Copolymer
Hydrogenated Rosin Glycerol Ester
Mineral Oil
Oleic Acid
Polyisobutylene
Polyester Film
Propylene Glycol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

label

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84763-01784763-017-01, 84763-017-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
TOLNAFTATE06KB629TKVACTIB
ETHYLENE-VINYL ACETATE COPOLYMER (50% VINYL ACETATE)3H390O24SIIACT
MINERAL OILT5L8T28FGPIACT
OLEIC ACID2UMI9U37CPIACT
POLYISOBUTYLENE (1000 MW)5XB3A63Y52IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCEROL ESTER OF HYDROGENATED ROSINXH62RP786NIACT
POLYETHYLENE TEREPHTHALATE (INTRINSIC VISCOSITY 0.60-0.70)5YSH70HE6KIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT

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 PATCHESTOLNAFTATEYunqi Cosmetics (Shenzhen) Co., Ltd5939c492-6481-ddae-e063-6294a90a40bb2026-08-17WarningsExact identifier
ndc (package): 84763-017-02
ndc (package): 84763-017-01
ndc (product): 84763-017
ndc11 (package): 84763001701
ndc11 (package): 84763001702
spl id: 5939c492-6482-ddae-e063-6294a90a40bb
spl set id: 5939c492-6481-ddae-e063-6294a90a40bb

Reported adverse events (FAERS/openFDA)#

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