THE PURE LOTUS Jeju Lotus Leaf Brightening Serum

Manufacturer
THE LOTUS Co.,Ltd.
Effective date
2021-09-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:36:09

Label at a glance#

ProductTHE PURE LOTUS Jeju Lotus Leaf Brightening Serum
Active ingredientNIACINAMIDE
Label structure11 sections

Indications and uses

Functional cosmetics for brightening.

Storage and handling

Store at room temperature away from direct sunlight.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Niacinamide (2%)

Purpose

OTC - PURPOSE SECTION

Brightening

Uses

DOSAGE & ADMINISTRATION SECTION

Functional cosmetics for brightening.

Warnings

WARNINGS SECTION

For external use only

Stop use and ask doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms last more than 7days or clear up and occur again within a few days

Do not use

OTC - DO NOT USE SECTION

  • Do not apply to wounds or damaged skin
  • In case of abnormal symptoms or side effects of red spots, swelling, or itching
  • Do not get into eyes

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Direction

INDICATIONS & USAGE SECTION

At the next step after washing face in the morning and the after washing face in the morning and the evening, take a suitable amount of serum, evening, take a suitable amount of serum, and softly spread it along with your skin and softly spread it along with your skin texture and let it absorbed.

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature away from direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water
Aloe Barbadensis Leaf Extract
Camellia Sinensis Leaf Extract
Nelumbo Nucifera Leaf Extract
Oryza Sativa (Rice) Extract
Citrus Unshiu Peel Extract
Rosmarinus Officinalis (Rosemary) Leaf Extract
Nelumbo Nucifera Root Extract
1,2-Hexanediol
Opuntia Coccinellifera Fruit Extract
Glycerin
Methyl Gluceth-20
Glyceryl Acrylate/Acrylic Acid Copolymer
Butylene Glycol
Propylene Glycol
Hydrogenated Lecithin
Agar
Poloxamer 407
Glyceryl Polymethacrylate
Synthetic Fluorphlogopite
Macrocystis Pyrifera (Kelp) Extract
Caprylyl Glycol
Ethylhexylglycerin
Titanium Dioxide (CI 77891)
Soluble Collagen
Dipropylene Glycol
Sodium Lactate
CI 77491
Retinyl Palmitate
Helianthus Annuus (Sunflower) Seed Oil
Tin Oxide (CI 77861)
Acetyl Hexapeptide-8
Tocopherol
Palmitoyl Tripeptide-1
BHT
Niacinamide
Cetearyl Olivate
Sorbitan Olivate
Sophora Angustifolia Root Extract
Citrus Junos Fruit Extract
Eucalyptus Globulus Leaf Extract
Citrus Paradisi (Grapefruit) Fruit Extract
Eugenia Caryophyllus (Clove) Flower Extract
Butyrospermum Parkii (Shea) Butter
Acrylates/C10-30 Alkyl Acrylate Crosspolymer
Arginine
Mallotus Japonicus Bark Extract
Fragrance
Benzyl Salicylate
Amyl Cinnamal
Butylphenyl Methylpropiona

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82235-30182235-301

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82235-30182235-301-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 48 matching rows.

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
edf77c7b-6f24-bd37-e053-2a95a90aea22cbf132c5-dc09-1554-e053-2a95a90a7d012022-11-21WarningsExact identifier
spl set id: cbf132c5-dc09-1554-e053-2a95a90a7d01

Reported adverse events (FAERS/openFDA)#

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