FDA.reportPublic FDA data

MORKORIA BEE VENOM WART REMOVER

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2025-09-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:34:40

Label at a glance#

ProductMORKORIA BEE VENOM WART REMOVER
Active ingredientSALICYLIC ACID, APIS MELLIFERA VENOM
Label structure12 sections

Dosage and administration

1.Wash the affected area. (soaking in warm water for 5 minutes may help.) 2. Dry thoroughly. 3. Apply a small amount to cover each wart. Let it dry 4. Repeat twice daily as needed, for up to 12 weeks.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 17% Bee venom 1%

Purpose

OTC - PURPOSE SECTION

Wart remover
Skin Repair

Use

INDICATIONS & USAGE SECTION

For the removal of common warts, for Plantar Wart, Corns,Flat Warts and Skin Tag.

Warnings

WARNINGS SECTION

For external use only-Avoid contact with eyes.
If the product gets into eyes, rinse with water for 15 minutes.Avoid inhalingvapors.

Do not use

OTC - DO NOT USE SECTION

On irritated or infected skin, or reddened areas.
lf you are diabetic or have poor blood circulation.
On birthmarks, warts with hair growth or moles

When Using

OTC - WHEN USING SECTION

If pregnant or breast feeding, consult a health professional before use.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if discomfort persists.

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if discomfort persists.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek immediate medical help or contact a Poison Control Center.

Directions

DOSAGE & ADMINISTRATION SECTION

1.Wash the affected area.
(soaking in warm water for 5 minutes may help.) 2. Dry thoroughly. 3. Apply a small amount to cover each wart. Let it dry 4. Repeat twice daily as needed, for up to 12 weeks.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Polyethylene Glycol, Glycerin, Borneol，Methylparaben，Chlorhexidine

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1717

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-17984010-179-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
BORNEOLM89NIB437XIACT
SALICYLIC ACIDO414PZ4LPZACTIB
METHYLPARABENA2I8C7HI9TIACT
CHLORHEXIDINER4KO0DY52LIACT
APIS MELLIFERA VENOM76013O881MACTIB
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT

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
4a47f188-be5a-42d3-e063-6394a90aa7833e1e88be-2d9f-9d6c-e063-6394a90af7632026-02-07WarningsExact identifier
spl set id: 3e1e88be-2d9f-9d6c-e063-6394a90af763

Reported adverse events (FAERS/openFDA)#

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