Mefactory Piggy Nose Pore Strip

Manufacturer
MeFactory Co., Ltd.
Effective date
2017-08-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:09

Label at a glance#

ProductMefactory Piggy Nose Pore Strip
Active ingredientWitch Hazel
Label structure8 sections

Indications and uses

Uses: Wet your nose with warm water and place the strip with dry hands. Let dry for 10 minutes until stiff to the touch and slowly peel off starting at the edge, 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 and administration

Directions: Suggested use is 1-2 times a week

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, 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

Uses

INDICATIONS & USAGE SECTION

Uses: Wet your nose with warm water and place the strip with dry hands. Let dry for 10 minutes until stiff to the touch and slowly peel off starting at the edge, 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions: Suggested use is 1-2 times a week

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70908-140-022020-01-31C16284748780-19d75b9d0-b836-f424-e053-dadaa90a57ce778e9997-9ecc-40d1-a88e-1874026b49fc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70908-140-01Mefactory Piggy Nose Pore Strip0.2 g in 1 POUCHPATCH0.21
70908-140-02Mefactory Piggy Nose Pore Strip10 in 1 CARTONPATCH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70908-140MEFACTORY PIGGY NOSE PORE STRIP (WITCH HAZEL) PATCH [MEFACTORY CO., LTD.]1Legacy NDC, 2 package rows20170808_778e9997-9ecc-40d1-a88e-1874026b49fc.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
70908-14070908-140-01, 70908-140-02

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

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
16a78d98-c28c-4108-8f1a-52a7a5860d0b778e9997-9ecc-40d1-a88e-1874026b49fc2017-08-08WarningsExact identifier
spl id: 16a78d98-c28c-4108-8f1a-52a7a5860d0b
spl set id: 778e9997-9ecc-40d1-a88e-1874026b49fc

Reported adverse events (FAERS/openFDA)#

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