TENSION NO. 5

Manufacturer
Maywell Co., Ltd. | Kolmar Korea Co.,LTD. Gwanjeong Factory
Effective date
2019-12-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:02:09

Label at a glance#

ProductTENSION NO. 5
Active ingredientWITCH HAZEL
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: HAMAMELIS VIRGINIANA (WITCH HAZEL) WATER 0.0002%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: WATER, BUTYLENE GLYCOL, ARGININE HCL, GLUTAMINE, LYSINE HCL, CAPRYLIC/CAPRIC TRIGLYCERIDE, HYDROGENATED LECITHIN, HYALURONIC ACID, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, POLYSORBATE 80, COMMIPHORA MYRRHA LEAF CELL EXTRACT, NELUMBO NUCIFERA LEAF EXTRACT, PYRUS MALUS (APPLE) FRUIT EXTRACT, JASMINUM SAMBAC (JASMINE) LEAF CELL EXTRACT, BIFIDA FERMENT LYSATE, RAFFINOSE, ARCTIUM LAPPA ROOT EXTRACT, PEG-60 HYDROGENATED CASTOR OIL, POLYQUATERNIUM-51, LECITHIN, GLYCERIN, CAPRYLYL GLYCOL, 1,2-HEXANEDIOL, SODIUM HYALURONATE, ANTHEMIS NOBILIS FLOWER WATER, BETA-GLUCAN, CENTAUREA CYANUS FLOWER WATER, EPILOBIUM ANGUSTIFOLIUM FLOWER/LEAF/STEM EXTRACT, INOSITOL, MAGNOLIA OFFICINALIS BARK EXTRACT, PSEUDOALTEROMONAS FERMENT EXTRACT, BHT, FRAGRANCE, PHELLINUS LINTEUS EXTRACT, ADENOSINE, DISODIUM EDTA, POTASSIUM SORBATE, FOLIC ACID, CERAMIDE 3, CHOLESTEROL, DIOSGENIN, ACETIC ACID, LACTIC ACID, ALCOHOL, TROMETHAMINE, PANTHENOL, PHENOXYETHANOL, DIPEPTIDE-2, COPPER TRIPEPTIDE-1, PALMITOYL TRIPEPTIDE-5, ACETYL HEXAPEPTIDE-8, PALMITOYL PENTAPEPTIDE-4, PALMITOYL TETRAPEPTIDE-7, ACETYL TRIPEPTIDE-1, PALMITOYL TRIPEPTIDE-1

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. In case of having following symptoms after using this, you’re advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problems such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of babies and children

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: After washing your face in the morning and evening, spray it on your face five time and on your neck three times as the first step of skin care. After patting it in gently with your hands, spray it on your face five times and on your neck three times again and let it absorb into the skin.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Five times in the face, neck three times

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of cartonImage of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69628-010-012022-01-28C16284748780-1d6a99b39-6b82-a426-e053-dadaa90af4c2db8d557d-b3cc-4610-be0c-31240df9e68d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69628-010-01TENSION NO. 550 mL in 1 CARTONCREAM505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69628-010TENSION NO. 5 (WITCH HAZEL) CREAM [MAYWELL CO., LTD.]5Legacy NDC, 1 package rows20191220_db8d557d-b3cc-4610-be0c-31240df9e68d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
WITCH HAZELACTIVE INGREDIENT101I4J0U342
WITCH HAZELACTIVE MOIETY101I4J0U342
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA2
WATERINACTIVE INGREDIENT059QF0KO0R2

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
69628-01069628-010-01

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
BUTYLENE GLYCOL3XUS85K0RAIACT

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
BUTYLENE GLYCOLBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
b246293b-3fd2-4d5a-8d06-274c91c87df0db8d557d-b3cc-4610-be0c-31240df9e68d2019-12-20WarningsExact identifier
spl id: b246293b-3fd2-4d5a-8d06-274c91c87df0
spl set id: db8d557d-b3cc-4610-be0c-31240df9e68d

Reported adverse events (FAERS/openFDA)#

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