Water Full Daily Mask

Manufacturer
MODECOS CO., LTD.
Effective date
2016-03-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:34

Label at a glance#

ProductWater Full Daily Mask
Active ingredientWitch Hazel
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: Hamamelis Virginiana (Witch Hazel) Leaf Extract 0.1%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, 1,2-Hexanediol, Glycereth-26, Butylene Glycol, Propylene Glycol, Betaine, Bis-PEG-18 Methyl Ether Dimethyl Silane, Arginine, Carbomer, PEG-60 Hydrogenated Castor Oil, Allantoin, Hydrolyzed Collagen, Sea Water, Disodium EDTA, Ceramide 3, Hydrogenated Lecithin, Dipotassium Glycyrrhizate, Dipropylene Glycol, Prunus Amygdalus Dulcis (Sweet Almond) Oil, rh-Oligopeptide-1, Glycereth-20, PEG-10 Rapeseed Sterol, Sodium Hyaluronate, Glyceryl Stearate, rh-Oligopeptide-2, rh-Polypeptide-1, rh-Polypeptide-3

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

Warnings: 1. If the following symptoms arise upon use of the cosmetic product, immediately discontinue use and consult a dermatologist, for continued use may aggravate the symptoms. A. Redness, swelling, itchiness, stimulation, or other symptoms B. Occurrence of the above symptoms upon exposure to direct sunlight. 2. Do not use on areas with wounds, eczema, or dermatitis. 3. Caution for storing. A. Put the lid back after using it. B. Keep it out of infants or children’s reach C. Don’t Keep it in the place where the temperature is extremely hot or cold and exposed to the direct sunlight D. Avoid using around the eye area.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep it out of infants or children’s reach

INDICATIONS & USAGE

INDICATIONS & USAGE SECTION

Indications & Usage: 1. After washing, prepare for mask treatment and tone skin by moisturizing your skin 2. Wear the mask, follow the cutting leave the eyes and mouth a space 3. Leave the mask 10 to 20 minutes and take it off. 4. Massage and dab the face gently let the essence absorb into skin cell well.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage & Administration: Use immediately after opening. 2-3 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
70566-020-012020-01-31C16284748780-19d75b9d0-7741-f424-e053-dadaa90a57ce40bb28fc-12b1-4f54-8001-0296ffbbf13c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70566-020-01Water Full Daily Mask10 in 1 CARTONSOLUTION101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70566-020WATER FULL DAILY MASK (WITCH HAZEL) SOLUTION [MODECOS CO., LTD.]1Legacy NDC, 1 package rows20160329_40bb28fc-12b1-4f54-8001-0296ffbbf13c.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
70566-02070566-020-01

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
1,2-HexanediolTR046Y3K1GIACT

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
04646f3e-0686-4fa8-bf89-f40e9d8d4d2f40bb28fc-12b1-4f54-8001-0296ffbbf13c2016-03-29WarningsExact identifier
spl id: 04646f3e-0686-4fa8-bf89-f40e9d8d4d2f
spl set id: 40bb28fc-12b1-4f54-8001-0296ffbbf13c

Reported adverse events (FAERS/openFDA)#

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