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Yehoyod Wart Remover Patches drug information

SALICYLIC ACID 40%
Shenzhen Xuesiang Trading Co., Ltd · TOPICAL

Product NDC: 87323-002

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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 nameSALICYLIC ACID 40%
Labeler / manufacturerShenzhen Xuesiang Trading Co., Ltd
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC87323-002
Label effective date2026-09-01

Official product label reference

Yehoyod Wart Remover Patches — Shenzhen Xuesiang Trading Co., Ltd

This page contains 9 source sections for SALICYLIC ACID 40%, topical route. Label set 5a774348-64e6-5cbe-e063-6294a90a7a2b, 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

For the removal of common and plantar warts.

Purpose

Wart remover
Dosage and administration — label text
Wash the affected area and dry thoroughly. Apply the medicated patch directly over the wart. Leave on for up to 48 hours. After removal, wash the affected area with warm water. Repeat as needed for up to 12 weeks. Small warts (1-3 mm) typically shed within 30 days with a success rate of over 90%; medium warts (3-5 mm) gradually dry and fall off within 60 days, with no recurrence reported.
Warnings
For external use only.
Active ingredient
Salicylic Acid 40%
Do not use
Do not use on moles, birthmarks, unusual warts with hair growing from them, or genital warts. Avoid contact with eyes, mouth, nostrils, and other mucous membranes. If contact occurs, rinse thoroughly with water. ​Do not apply to broken skin or healthy skin surrounding the wart.
When to stop use and seek help
May cause irritation. Discontinue use if severe discomfort or sensitivity occurs.
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Inactive ingredient
SOPHORA FLAVESCENS ROOT DICTAMNUS DASYCARPUS ROOT PURSLANE LITHOSPERMUM ERYTHRORHIZON ROOT BASSIA SCOPARIA FRUIT PRUNUS MUME FRUIT RHUS CHINENSIS GALL BORNEOL CAMPHOR(NATURAL)

Official sources and product identifiers

Substances listed: SALICYLIC ACID

RxNorm identifiers: 240559

Package NDC codes

87323-002-01

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.