FDA.reportPublic FDA data

Mole Reduce Essence

Manufacturer
TT Beauty Trading Co., Ltd.
Effective date
2025-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:41:55

Label at a glance#

ProductMole Reduce Essence
Active ingredientALOE BARBADENSIS LEAF, CENTELLA ASIATICA LEAF, HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER
Label structure12 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

CENTELLA ASIATICA EXTRACT、
HAMAMELIS VIRGINIANA (WITCH HAZEL) EXTRACT、
ALOE BARBADENSIS EXTRACT

OTC - PURPOSE SECTION

Don't Be Embarrassed By Skin Tags.

Make Your Skin Smooth.

OTC - WHEN USING SECTION

1. Clean and dry the affected area. 2. Take an appropriate amount of essence. 3. Apply the essence to the surrounding skin. 4. Apply 2 times a day.

WARNINGS SECTION

Please keep out of reach of children. Do not swallow. Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children. Do not swallow.

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

AQUA、
GLYCERIN

DOSAGE & ADMINISTRATION SECTION

1. Clean and dry the affected area. 2. Take an appropriate amount of essence. 3. Apply the essence to the surrounding skin. 4. Apply 2 times a day.

INDICATIONS & USAGE SECTION

1. Clean and dry the affected area. 2. Take an appropriate amount of essence. 3. Apply the essence to the surrounding skin. 4. Apply 2 times a day.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85206-009-01Mole Reduce Essence30 mg in 1 BOTTLELIQUID301

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85206-00985206-009-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE BARBADENSIS LEAFZY81Z83H0XACTIB
CENTELLA ASIATICA LEAF6810070TYDACTIB
GLYCERINPDC6A3C0OXIACT
AQUA059QF0KO0RIACT
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER8FP93ED6H2ACTIB

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
42a82dc1-0584-caba-e063-6294a90a46a542a82dc1-0583-caba-e063-6294a90a46a52025-11-02WarningsExact identifier
spl id: 42a82dc1-0584-caba-e063-6294a90a46a5
spl set id: 42a82dc1-0583-caba-e063-6294a90a46a5

Reported adverse events (FAERS/openFDA)#

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