FDA.reportPublic FDA data

WART REMOVER

Manufacturer
Shenzhen Derbit Technology Co., Ltd.
Effective date
2024-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:07:32

Label at a glance#

ProductWART REMOVER
Active ingredientSALIX ALBA BARK, IMPATIENS BALSAMINA FLOWER, REHMANNIA GLUTINOSA ROOT, ACETIC ACID, AMINO ACIDS, HAIR KERATIN, DICTAMNUS DASYCARPUS ROOT BARK, PANAX NOTOGINSENG ROOT, SOPHORA FLAVESCENS ROOT
Label structure12 sections

Storage and handling

Other Information ( Storage and Processing Section ) Edit Store at 10-30 ( 59-86F )

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chinese rehmannia ( REHMANNIACHINENSIS ) root extract 3%

Sophora flavescens ( SOPHORAFLAVESCENS ) extrac 3%

White Willow ( SALIX ALBA ) BarkExtract 2%

Acetic acid 1%

Keratin 0.5%

Impatiens balsamina flowerextract 3%

White fresh ( DICTAMNUSDASYCARPUS ) root bark extract 2%

Panax notoginseng ( PANAXNOTOGINSENG ) extract 2%

purpose

OTC - PURPOSE SECTION

enhance skin metabolism

antibacterial andanti-inflammatory

Anti-inflammatory

reduce fungalinfection

promote nailgrowth

promoting bloodcirculation and relieving pain

antipruritic

stopbleeding, enhance immunity

use

INDICATIONS & USAGE SECTION

Reduces fungal infections on nailsand helps restore nails to health.

Warning

WARNINGS SECTION

For external use only, do not consume

Do not use

OTC - DO NOT USE SECTION

Do not use under open wounds

When using SECTION

OTC - WHEN USING SECTION

When using this product, keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water. If irritation or rash occurs, discontinue use and ask a doctor. These may be signs of a serious condition Please keep this product out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC-STOP USE SECTION

OTC - STOP USE SECTION

If irritation or rash occurs, discontinue useand ask a doctor.

These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep this product out of the reach ofchildren. If swallowed, get medical help orcontact a Poison Control Center right away.

Direction

DOSAGE & ADMINISTRATION SECTION

Spread the product over the nail fungus andwait for the product to be absorbed .When using this product , supervise childrenunder 6 years of age to avoid swallowing .Other Information ( Storage and ProcessingSection ) Edit Store at 10-30 ( 59-86F )

STORAGE AND HANDLING SECTION

Other Information ( Storage and Processing Section ) Edit Store at 10-30 ( 59-86F )

inactive ingredients

INACTIVE INGREDIENT SECTION

Water , Glycerin , Xanthan Gum, Methylparaben , Caprylyl Hydroxamic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83619-001-0183619-001-01

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
48747306-602a-42cc-957b-5b0c69158eeeProduct name120180604
db5ebcdb-b6ae-21cd-4dc5-76cd84b5578bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83619-001-012025-07-29C16284748780-13b156c62-324d-fb37-e063-e6dba90a4e0702881c00-8a85-22eb-e063-6294a90a7fdc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83619-001-01WART REMOVER10 mL in 1 BOXLIQUID102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83619-001WART REMOVER LIQUID [SHENZHEN DERBIT TECHNOLOGY CO., LTD.]21 package rows20240119_02881c00-8a85-22eb-e063-6294a90a7fdc.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83619-00183619-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALIX ALBA BARK205MXS71H7ACTIB
IMPATIENS BALSAMINA FLOWER3169PS5TJHACTIB
CAPRYLHYDROXAMIC ACIDUPY805K99WIACT
REHMANNIA GLUTINOSA ROOT1BEM3U6LQQACTIB
ACETIC ACIDQ40Q9N063PACTIB
AMINO ACIDS, HAIR KERATING46579QK1MACTIB
DICTAMNUS DASYCARPUS ROOT BARKLA97176ILSACTIB
PANAX NOTOGINSENG ROOTGQX1C1175UACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
XANTHAN GUMTTV12P4NEEIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KACTIB
METHYLPARABENA2I8C7HI9TIACT

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
0ea27d3e-101b-7f67-e063-6394a90a8f8a02881c00-8a85-22eb-e063-6294a90a7fdc2024-01-10WarningsExact identifier
spl id: 0ea27d3e-101b-7f67-e063-6394a90a8f8a
spl set id: 02881c00-8a85-22eb-e063-6294a90a7fdc

Reported adverse events (FAERS/openFDA)#

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