Wart Remover

Manufacturer
binzhoutengfenshangmaoyouxiangongsi
Effective date
2024-07-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:14:39

Label at a glance#

ProductWart Remover
Active ingredient3,5-DIBROMOSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid

Chlorhexidine acetate

OTC - PURPOSE SECTION

has the maximum performance for common, plantar, and genital warts.It is the natural choice for treating warts for the whole family.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INACTIVE INGREDIENT SECTION

PurifedWater,Witch Hazel ,ExtractPeppermint Extract,TeaTree oil

DOSAGE & ADMINISTRATION SECTION

30ml

1. Clean the skin before use, then wipe dry.

2. Shake this product well before use, use a smudge brush to take 1-2 drops of makeup remover and apply it on the miliary skin, let it fully absorb and dry completely

(Recommended to use twice a day until milia go away, which usually falls off within 7-14 days.)

CAUTION:This product is for external use only, not for internal use.

WARNINGS SECTION


1. store in cool dry place way from sunlight
2. Keep out of reach of children.

INDICATIONS & USAGE SECTION

1. Clean the skin before use, then wipe dry.

2. Shake this product well before use, use a smudge brush to take 1-2 drops of makeup remover and apply it on the miliary skin, let it fully absorb and dry completely

(Recommended to use twice a day until milia go away, which usually falls off within 7-14 days.)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
84510-123-022025-07-29C16284748780-13b156c62-2add-fb37-e063-e6dba90a4e071c563797-d3a5-14a1-e063-6294a90a0a21

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84510-123-01Wart Remover30 mL in 1 BOTTLELIQUID301
84510-123-02Wart Remover1 in 1 BOX, UNIT-DOSELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84510-123WART REMOVER LIQUID [BINZHOUTENGFENSHANGMAOYOUXIANGONGSI]12 package rows20240704_1c563797-d3a5-14a1-e063-6294a90a0a21.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84510-12384510-123-01, 84510-123-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
1c563797-d3a6-14a1-e063-6294a90a0a211c563797-d3a5-14a1-e063-6294a90a0a212024-07-03WarningsExact identifier
spl id: 1c563797-d3a6-14a1-e063-6294a90a0a21
spl set id: 1c563797-d3a5-14a1-e063-6294a90a0a21

Reported adverse events (FAERS/openFDA)#

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