Mefactory 3Step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet

Manufacturer
MeFactory Co., Ltd.
Effective date
2017-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:49:07

Label at a glance#

ProductMefactory 3Step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet
Active ingredientWitch Hazel
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Hamamelis Virginiana (Witch Hazel) Leaf Extract 0.01%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: PVP, Purified water, Glycerin, PEG-12 Dimethicone, Kaolin, Titanium Dioxide , VP/VA Copolymer, Butylene Glycol , Phenoxyethanol , Hydrolyzed Collagen , Nelumbo Nucifera Flower Extract, Portulaca Oleracea Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract , Camellia Sinensis Leaf Extract , Betula Platyphylla Japonica Juice, Sea Water , Bambusa Vulgaris Water , Jasminum Officinale (Jasmine) Flower Water , Rosa Damascena Flower Water

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: For external use only 1. Discontinue use immediately and consult a dermatologist, if you experience the following: 1) Irritation, Red spots, itchy skin or rash 2) Applied skin area has the above reaction from direct sun 2. Do not use on irritated skin, cuts, or other infected skin area. 3. Avoid contact with eyes.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: Wet your nose with warm water and place step2 with dry hands. Let dry for 10minutes until stiff to the touch and slowly and carefully peel off starting at deges, pulling toward center. For the best result, be sure to remove strip as directed promptly after it becomes stiff and do not get it wet again.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Suggested use is 1-2 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of pouchImage of pouch

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70908-090-012020-01-31C16284748780-19d75b9d0-287b-f424-e053-dadaa90a57cedc4ad196-d38b-40d4-b036-726d6eb9a581

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70908-090-01Mefactory 3Step Piggy Nose Pore Strip Step 02 Blackhead Clearing Sheet0.2 g in 1 POUCHPATCH0.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70908-090MEFACTORY 3STEP PIGGY NOSE PORE STRIP STEP 02 BLACKHEAD CLEARING SHEET (WITCH HAZEL) PATCH [MEFACTORY CO., LTD.]1Legacy NDC, 1 package rows20170303_dc4ad196-d38b-40d4-b036-726d6eb9a581.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70908-09070908-090-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Witch Hazel101I4J0U34ACTIB
WATER059QF0KO0RIACT
GlycerinPDC6A3C0OXIACT

Source Document#

Source XML · Source PDF

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
9451c712-4554-4fb4-94ec-5d9037afa457dc4ad196-d38b-40d4-b036-726d6eb9a5812017-03-03WarningsExact identifier
spl id: 9451c712-4554-4fb4-94ec-5d9037afa457
spl set id: dc4ad196-d38b-40d4-b036-726d6eb9a581

Reported adverse events (FAERS/openFDA)#

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