FDA.reportPublic FDA data

Pureskin Molluscum Treatment

Manufacturer
Stellans Inc.
Effective date
2023-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:28:46

Label at a glance#

ProductPureskin Molluscum Treatment
Active ingredientTHUJA OCCIDENTALIS LEAF
Label structure13 sections

Dosage and administration

Wash and dry the affected area. Apply the liquid to the bumps 3-4 times a day and let it dry. Continue the treatment daily until molluscum contagiosum disappears.

Storage and handling

store at 15-25 ℃

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Thuja Occidentalis 5x HPUS

Purpose

OTC - PURPOSE SECTION

Molluscum Symptom Relief

Use

INDICATIONS & USAGE SECTION

Relief for Molluscum Contagiosum symptoms, such as itch, bumps, and lesions.

Do not use

OTC - DO NOT USE SECTION

On open skin wounds

When Using

OTC - WHEN USING SECTION

Avoid contact with eyes. If contact occurs, rinse the eyes immediately with water.
Keep out of the reach of young children.

Stop Use

OTC - STOP USE SECTION

If you are allergic to this product.
If symptoms persist for over 7 days or worsen, consult your physician.
If you are pregnant or breast-feeding
You become pregnant or are planning to become pregnant while using this product

Ask Doctor

OTC - ASK DOCTOR SECTION

If you are allergic to this product.
If symptoms persist for over 7 days or worsen, consult your physician.
If you are pregnant or breast-feeding
You become pregnant or are planning to become pregnant while using this product

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.In case of ingestion, call Poison Control Center hotline immediately or seek medical help.

Directions

DOSAGE & ADMINISTRATION SECTION

Wash and dry the affected area.
Apply the liquid to the bumps 3-4 times a day and let it dry.
Continue the treatment daily until molluscum contagiosum disappears.

Other information

STORAGE AND HANDLING SECTION

store at 15-25 ℃

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water
Glycerin
Brucea Javanica
Cyperus Cyperinus
Equisetum
Peucedanum
Isatis Tinctoria Root

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

144144

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
83565-00283565-002-01

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
CYPERUS CYPERINUS WHOLEZJ537UL75OIACT
WATER059QF0KO0RIACT
PEUCEDANUM OSTRUTHIUM LEAF86P27YRR6YIACT
THUJA OCCIDENTALIS LEAF0T0DQN8786ACTIB
GLYCERINPDC6A3C0OXIACT
ISATIS TINCTORIA ROOT8S10GFI6DXIACT
EQUISETUM ARVENSE TOP1DP6Y6B65ZIACT
BRUCEA JAVANICA WHOLEZ4CCI5NZ66IACT

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
21aceda5-2c38-23df-e063-6394a90acb09006a523a-00c9-d74b-e063-6394a90a47682024-09-09WarningsExact identifier
spl set id: 006a523a-00c9-d74b-e063-6394a90a4768

Reported adverse events (FAERS/openFDA)#

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