Pureskin Molluscum Treatment by Stellans Inc. 83565-002 Completed

Pureskin Molluscum Treatment by

Drug Labeling and Warnings

Pureskin Molluscum Treatment by is a Otc medication manufactured, distributed, or labeled by Stellans Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURESKIN MOLLUSCUM TREATMENT- molluscum treatment liquid 
Stellans Inc.

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83565-002 Completed

Active Ingredient

Thuja Occidentalis 5x HPUS

Purpose

Molluscum Symptom Relief

Use

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

Warnings

Do not use

On open skin wounds

When Using

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

Stop Use

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

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

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

Directions

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

store at 15-25 ℃

Inactive ingredients

Water
Glycerin
Brucea Javanica
Cyperus Cyperinus
Equisetum
Peucedanum
Isatis Tinctoria Root

Questions

info@pureskinsupport.com
www.pureskinsupport.com

PRINCIPAL DISPLAY PANEL

PURESKIN MOLLUSCUM TREATMENT 
molluscum treatment liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83565-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786)	THUJA OCCIDENTALIS LEAF	5 [hp_X]  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CYPERUS CYPERINUS WHOLE (UNII: ZJ537UL75O)
WATER (UNII: 059QF0KO0R)
PEUCEDANUM OSTRUTHIUM LEAF (UNII: 86P27YRR6Y)
GLYCERIN (UNII: PDC6A3C0OX)
ISATIS TINCTORIA ROOT (UNII: 8S10GFI6DX)
EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
BRUCEA JAVANICA WHOLE (UNII: Z4CCI5NZ66)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83565-002-01	15 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/13/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	07/13/2023	09/09/2024

Labeler - Stellans Inc. (111157321)

Establishment
Name	Address	ID/FEI	Business Operations
Stellans Inc.		111157321	manufacture(83565-002) , label(83565-002)

Revised: 9/2024

Document Id: 21aceda5-2c38-23df-e063-6394a90acb09

34390-5

Set id: 006a523a-00c9-d74b-e063-6394a90a4768

Version: 2

Effective Time: 20240909