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Noicaky FUNGAL NAIL Patches drug information

TOLNAFTATE 1% FUNGAL NAIL PATCHES
Wenzhou Yuyuan Pharmaceutical Co., Ltd. · TOPICAL

Product NDC: 87786-059

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameTOLNAFTATE 1% FUNGAL NAIL PATCHES
Labeler / manufacturerWenzhou Yuyuan Pharmaceutical Co., Ltd.
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC87786-059
Label effective date2026-09-06

Official product label reference

Noicaky FUNGAL NAIL Patches — Wenzhou Yuyuan Pharmaceutical Co., Ltd.

This page contains 12 source sections for TOLNAFTATE 1% FUNGAL NAIL PATCHES, topical route. Label set 5adcc5f7-2d47-2ad7-e063-6294a90a4848, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use Repairs fungal nail damage and improves nail appearance

Purpose

Purpose Anti-Fungal
Dosage and administration — label text
Directions Directions: Clean and thoroughly dry the affected area before application. ■ Peel off the patch's protective film, starting with the outer side and then the inner side. ■ Place the sticky side of the patch directly onto the infected area on the nail and remove the release paper. Gently wrap the sides of the toe or finger to ensure a snug fit. ■ Fold the remaining adhesive part to cover the toe/fingertip. Leave the patch on for 6-8 hours (It is recommended to use overnight for 3-6 months).
Warnings
Warnings For external use only.
Active ingredient
Active Ingredient Tolnaftate l%
Do not use
Do not use Avoid direct contact with eyes, mouth, mucous membrane, wounds Do not use if you are allergic to any of the ingredients Do not use if you are pregnant or breastfeeding
While using this medicine
When Using Avoid direct contact with eyes, mouth, mucous membrane, wounds
When to stop use and seek help
Stop Use if irritation occurs and discomfort persists
Ask a doctor before use
Ask Doctor if you have diabetes or poor blood circulation
Child safety
Keep Out Of Reach Of Children In case of contact with eyes, flush with water for at least 15 minutes. If swallowed, seek medical assistance immediately or contact a Poison Control Center.
Storage and handling
Other information Store at room temperature and keep away from direct sunlight. Skin discoloration may occur during or after use.
Inactive ingredient
Inactive ingredients Water, Polyester Spandex, Acrylate Copolymer, Tackifying Resin, Glycerin, Silicone Oil Paper

Official sources and product identifiers

Substances listed: TOLNAFTATE

RxNorm identifiers: 2677690

Package NDC codes

87786-059-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.