FDA.reportPublic FDA data

Manefit Beauty Planner Lily Brightening Eye Mask

Manufacturer
Imine Co., Ltd.
Effective date
2016-04-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:27:35

Label at a glance#

ProductManefit Beauty Planner Lily Brightening Eye Mask
Active ingredientNIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Niacinamide 2.00%

OTC - PURPOSE SECTION

Skin Protectant

INDICATIONS & USAGE SECTION

An eye mask infused with lily extracts to brighten and hydrate the skin
around the eyes

DOSAGE & ADMINISTRATION SECTION

After cleansing and toning skin, lay the eye mask carefully around your eyes. Keep the eye mask in place for 30 minutes. Remove the eye mask and gently tap the skin lightly to absorb the essence.

WARNINGS SECTION

For external use only.
Do not use on damaged or broken skin.
When using this product, keep out of eyes. Rinse with water to remove
Stop using and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Glycerin, Cetyl Ethylhexanoate, Citrus Paradisi (Grapefruit) Fruit Extract, Lilium Tigrinum Extract, Ceratonia Siliqua Gum, Chondrus Crispus Powder, Glyceryl Stearate, Cellulose Gum, Sodium Polyacrylate, Hydrogenated Polydecene, Vitis Vinifera (Grape) Fruit Extract, Citrus Aurantium Dulcis (Orange) Fruit Extract, Pyrus Malus (Apple) Fruit Extract, Citrus Medica Limonum (Lemon) Fruit Extract, Citrus Aurantifolia (Lime) Fruit Extract, Trideceth-6, Hydrolyzed Collagen, Magnesium Ascorbyl Phosphate, Disodium EDTA, Phenoxyethanol, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59401-02459401-024-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4ACTIB
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXIACT
CETYL ETHYLHEXANOATE134647WMX4IACT
GRAPEFRUITO82C39RR8CIACT
LILIUM LANCIFOLIUM BULB47Z05W73EZIACT
LOCUST BEAN GUMV4716MY704IACT
CHONDRUS CRISPUSOQS23HUA1XIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORMK679OBS311IACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
HYDROGENATED POLYDECENE (550 MW)U333RI6EB7IACT
WINE GRAPE3GOV20705GIACT
ORANGE5EVU04N5QUIACT
APPLEB423VGH5S9IACT
LEMON24RS0A988OIACT
LIME (CITRUS)8CZS546954IACT
TRIDECETH-63T5PCR2H0CIACT
MAGNESIUM ASCORBYL PHOSPHATE0R822556M5IACT
EDETATE DISODIUM7FLD91C86KIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
9ab4ef4f-c1e5-982d-e053-2995a90a6e2bfe42bdde-56f0-411a-ae1c-20f2dda0f9a12019-12-27WarningsExact identifier
spl set id: fe42bdde-56f0-411a-ae1c-20f2dda0f9a1

Reported adverse events (FAERS/openFDA)#

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