FDA.reportPublic FDA data

BURRRER Wart Remover

Manufacturer
Shenzhen TeLaFaErJiaLuo Technology Co., Ltd.
Effective date
2025-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:02:53

Label at a glance#

ProductBURRRER Wart Remover
Active ingredientSALICYLIC ACID
Label structure13 sections

Dosage and administration

1.Dip the liquid with the brush and apply it on the affected area.Wait for turning to mask. 2.Continue daily application for at least 2 weeks until the skin appears smooth. 3.More severe may require more time

Storage and handling

Keep the bottle sealed and store it at a shady place.Avoid excessive heat (37°℃/99°F). Skin discoloration may occur during or after use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

salicylic acid 17%

Purpose

OTC - PURPOSE SECTION

WART & CORN REMOVER

Use

INDICATIONS & USAGE SECTION

For the removal of common warts and plantar warts.

Warnings

WARNINGS SECTION

For external use only.
Keep away from fire and flame.
only use on affected area.
Please keep outofreach ofchildren.

Do not use

OTC - DO NOT USE SECTION

on the facial or eye area.
on damaged or cut skin,like wounds,grazes,eczema,sunburn,etc.
lf you have a known allergy to this product.

When Using

OTC - WHEN USING SECTION

When using,keep out of eyes,ears, mouth and any open hurt skin area.
In case of contact with eyes,rinse eyes thoroughly with water.

Stop Use

OTC - STOP USE SECTION

Stop using and ask a doctor if irritation or rash occurs.

Ask Doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you are Pregnant breastfeeding
Children over three years old should use it under adult supervision,and those under three years old should
consult a doctor first.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed,get medical help or contact a Poison Control Center（1-800-222-1222)right away.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Dip the liquid with the brush and apply it on the affected area.Wait for turning to mask.
2.Continue daily application for at least 2 weeks until the skin appears smooth.
3.More severe may require more time

Other information

STORAGE AND HANDLING SECTION

Keep the bottle sealed and store it at a shady place.Avoid excessive heat (37°℃/99°F).
Skin discoloration may occur during or after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,propylene glycol,ethanol, frutus cnidii, kuh-seng, purslane, rhizome of large-headed atractylodes, root of Dahurian
angelica, dried orange peel, xanthan gum.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312881salicylic acid 17 % Topical SolutionPSN1
312881salicylic acid 170 MG/ML Topical SolutionSCD1
312881salicylic acid 17 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85795-001-01BURRRER Wart Remover30 mL in 1 BOTTLELIQUID301

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85795-00185795-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ANGELICA DAHURICA ROOT1V63N2S972IACT
SALICYLIC ACIDO414PZ4LPZACTIB
TANGERINE PEELJU3D414057IACT
XANTHAN GUMTTV12P4NEEIACT
ACETALDEHYDEGO1N1ZPR3BIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
GLYCOLFC72KVT52FIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
PURSLANEM6S840WXG5IACT
ATRACTYLODES MACROCEPHALA WHOLE61Q25TS7LHIACT

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
BURRRER Wart RemoverWART REMOVERShenzhen TeLaFaErJiaLuo Technology Co., Ltd.374735f6-426d-8fe5-e063-6394a90ab2b82025-06-11WarningsExact identifier
ndc (package): 85795-001-01
ndc (product): 85795-001
ndc11 (package): 85795000101
spl id: 374735f6-426e-8fe5-e063-6394a90ab2b8
spl set id: 374735f6-426d-8fe5-e063-6394a90ab2b8

Reported adverse events (FAERS/openFDA)#

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