Neatique Bee Venom Wart Corn Treatment Liquid

Manufacturer
Shenzhen Zealous Ecommerce Technology Co., Ltd
Effective date
2025-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:36:55

Label at a glance#

ProductNeatique Bee Venom Wart Corn Treatment Liquid
Active ingredientCENTELLA ASIATICA TRITERPENOIDS, SODIUM HYALURONATE, ACETIC ACID, SALICYLIC ACID, APIS MELLIFERA VENOM, MELALEUCA ALTERNIFOLIA LEAF, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
Label structure14 sections

Dosage and administration

Only for adults. Cleanse: Wash the affected area with soap and water. Pat dry. Soak (optional): Soak wart in warm water for 5 minutes to soften. Apply: Using the applicator tip, place 1–2 drops directly onto the wart until fully covered. Let dry. Repeat: Use 1–2 times daily. Maximum treatment duration: 12 weeks. Post-treatment: Discontinue once the wart and surrounding dead tissue detach.

Storage and handling

Storage: Tighten cap after use. Store in a cool, dry place. Avoid exposure to temperatures above 37°C (99°F). Possible Side Effects: Temporary skin irritation, redness, or peeling at the application site. Darkening or lightening of the skin may occur; consult a doctor if persistent. Hygiene Tip: Clean the tube nozzle with a clean tissue after each use to prevent clogging.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Apis Mellifera Venom Extract 18%
Hamamelis Virginiana Extract 5%
Melaleuca Alternifolia Extract 4%
Centella Asiatica Extract 3.5%
Glacial Acetic Acid 2.2%
Salicylic Acid 2%
Sodium Hyaluronate 1%

Purpose

OTC - PURPOSE SECTION

Apis Mellifera Venom Extract 18% - Anti-inflammatory
Hamamelis Virginiana Extract 5% - Fights Bacteria
Melaleuca Alternifolia Extract 4% - Tightens Pores
Centella Asiatica Extract 3.5% - Soothes Skin
Glacial Acetic Acid 2.2% - pH Balancing
Salicylic Acid 2% - Wart Remover
Sodium Hyaluronate 1% - Intense Hydration

Use

INDICATIONS & USAGE SECTION

Removes: Common warts: Rough, raised growths with a "cauliflower-like" texture, typically on hands, fingers, or knees. Plantar warts: Hard, flat lesions on the soles of the feet, often tender and surrounded by thickened skin.

Warnings

WARNINGS SECTION

Safety Precautions: Flammable: Keep away from flames, sparks, or heat sources. External use only.

Do not use

OTC - DO NOT USE SECTION

Do not use if you are allergic to any of the ingredients. Do not use if you have diabetes, peripheral artery disease, or poor circulation.

When Using

OTC - WHEN USING SECTION

When using this product do not get into eyes.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if severe pain, swelling, or bleeding develops.

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if severe pain, swelling, or bleeding develops.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

Directions

DOSAGE & ADMINISTRATION SECTION

Only for adults. Cleanse: Wash the affected area with soap and water. Pat dry. Soak (optional): Soak wart in warm water for 5 minutes to soften. Apply: Using the applicator tip, place 1–2 drops directly onto the wart until fully covered. Let dry. Repeat: Use 1–2 times daily. Maximum treatment duration: 12 weeks. Post-treatment: Discontinue once the wart and surrounding dead tissue detach.

Other information

STORAGE AND HANDLING SECTION

Storage: Tighten cap after use. Store in a cool, dry place. Avoid exposure to temperatures above 37°C (99°F). Possible Side Effects: Temporary skin irritation, redness, or peeling at the application site. Darkening or lightening of the skin may occur; consult a doctor if persistent. Hygiene Tip: Clean the tube nozzle with a clean tissue after each use to prevent clogging.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerol, Ppg-2-Ceteareth-9, Phenoxyethanol

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85587-00485587-004-01

Ingredients#

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

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

Source Document#

Source XML

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5264d219-ae04-d945-e063-6394a90a49b6376034a0-6698-d652-e063-6294a90ae8772026-05-22WarningsExact identifier
spl set id: 376034a0-6698-d652-e063-6294a90ae877

Reported adverse events (FAERS/openFDA)#

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