QQE WART REMOVER

Manufacturer
Hainan Shengtaizhuo International Information Development Co., LTD
Effective date
2025-10-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:38:05

Label at a glance#

ProductQQE WART REMOVER
Active ingredientSALICYLIC ACID
Label structure11 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

WART REMOVER

OTC - ACTIVE INGREDIENT SECTION

20% SALICYLIC ACID

INDICATIONS & USAGE SECTION

1. Clean the affected area.
2. Dip a cotton swab in a small amount of the liquid medicine and apply it only to the surface of the wart, avoiding contact with the surrounding skin.
3. You can apply moisturizing cream around the wart.
4. Let it air dry naturally after application and avoid friction or covering with clothing.

WARNINGS SECTION

For external use only.For external use only Keep away from fire and flame

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

1. Do not apply on other parts of the body, For topical use only on the scalp
2. Avoid contact with the eyes in case of accidental contact rinse eyes with large arnounts of cool tap water.

OTC - DO NOT USE SECTION

You are under 18 years old. Do not use it for infants and children. Red, inflamed, infected, itchy or painful scalp.
You are using other medications on the affected area. If you have heart disease, consult your doctor before using.

OTC - STOP USE SECTION

Chest pain, rapid heart beat, faintness, or dizziness occurs sudden, unexplained weight gain occurs,your hands or feet swell.

DOSAGE & ADMINISTRATION SECTION

Twice each day,4 sprays (1ml)each time. 30 days supply

INACTIVE INGREDIENT SECTION

WATER, BORNEOL, GLYCERIN, PODOFILOX, POLYETHYLENE GLYCOL, BISABOLOL, ALLANTOIN.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WART REMOVERWART REMOVER

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a90fd6c4-df39-45aa-ddf9-e6c34fff3951Product name220250805
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
22fe7b8d-6b80-a6ee-3b72-558f5763c606Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84556-425-01QQE WART REMOVER30 mL in 1 BOTTLE, PLASTICLIQUID302

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
84556-42584556-425-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
QQE WART REMOVERSALICYLIC ACIDHainan Shengtaizhuo International Information Development Co., LTD3ed1e679-53ab-541c-e063-6294a90a2bec2025-10-07WarningsExact identifier
ndc (package): 84556-425-01
ndc (product): 84556-425
ndc11 (package): 84556042501
spl id: 408ec293-8fa3-dd4d-e063-6294a90ae1fc
spl set id: 3ed1e679-53ab-541c-e063-6294a90a2bec

Reported adverse events (FAERS/openFDA)#

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