FDA.reportPublic FDA data

LUPIUM MOISTURE WATER SUN SERUM

Manufacturer
JYOONCOSMETICS Co, Ltd | Cosmax, Inc.
Effective date
2021-10-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:42:42

Label at a glance#

ProductLUPIUM MOISTURE WATER SUN SERUM
Active ingredientNiacinamide, Titanium Dioxide, Adenosine, Zinc Oxide
Label structure9 sections

Indications and uses

Helps in brightening the skin. Helps in anti-wrinkles on the skin. Protects the skin from UV rays

Dosage and administration

At the last step of skin care, take an appropriate amount and apply it thoroughly along the skin texture.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Niacinamide 2%
Titanium Dioxide 1.73%
Adenosine 0.04%
Zinc Oxide 0.01%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Dibutyl Adipate, Phenethyl Benzoate, Butylene Glycol, Butyloctyl Salicylate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Diphenylsiloxy Phenyl Trimethicone, Polysilicone-15, Alcohol, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Ethylhexyl Triazone, Diethylhexyl Butamido Triazone, C12-15 Alkyl Benzoate, 1,2-Hexanediol, Pentylene Glycol, Sodium Acrylates Crosspolymer-2, C14-22 Alcohols, C20-22 Alkyl Phosphate, Polyglyceryl-3 Distearate, C20-22 Alcohols, Decyl Glucoside, Hydroxyacetophenone, Potassium Cetyl Phosphate, Silica, C12-20 Alkyl Glucoside, Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aluminum Hydroxide, Fragrance(Parfum), Glycerin, Glyceryl Stearate Citrate, Sodium Phytate, Isostearic Acid, Polyhydroxystearic Acid, Xanthan Gum, Squalane, Sodium Hyaluronate, Glyceryl Caprylate, Ceramide NP, Hydroxypropyltrimonium Hyaluronate, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Potassium Hyaluronate, rh-Oligopeptide-1, rh-Oligopeptide-2, rh-Polypeptide-1

PURPOSE

OTC - PURPOSE SECTION

Brightening, Sunscreen, Anti-wrinkles

WARNINGS

WARNINGS SECTION

For external use only
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Replace the cap after use.
Keep out of reach of children

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Uses

INDICATIONS & USAGE SECTION

Helps in brightening the skin.
Helps in anti-wrinkles on the skin.
Protects the skin from UV rays

Directions

DOSAGE & ADMINISTRATION SECTION

At the last step of skin care, take an appropriate amount and apply it thoroughly along the skin texture.

QUESTIONS

OTC - QUESTIONS SECTION

If there is any problem with this product, please contact us at the email address below. Customer Service : cscenter@skinisgood.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ADENOSINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82284-010-022023-01-30C16284748780-1f386c649-d016-0266-e053-dadaa90a7c1adab24235-3648-4c22-9999-82b2a146efef

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82284-010-01LUPIUM MOISTURE WATER SUN SERUM50 mL in 1 CONTAINERLIQUID501
82284-010-02LUPIUM MOISTURE WATER SUN SERUM1 in 1 CARTONLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82284-010LUPIUM MOISTURE WATER SUN SERUM (NIACINAMIDE, TITANIUM DIOXIDE, ADENOSINE, ZINC OXIDE) LIQUID [JYOONCOSMETICS CO, LTD]1Legacy NDC, 2 package rows20211013_dab24235-3648-4c22-9999-82b2a146efef.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82284-01082284-010-01, 82284-010-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
Niacinamide25X51I8RD4ACTIB
Titanium Dioxide15FIX9V2JPACTIB
AdenosineK72T3FS567ACTIB
Zinc OxideSOI2LOH54ZACTIM
Water059QF0KO0RIACT
Dibutyl AdipateF4K100DXP3IACT

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
f5a14b59-3491-4585-a559-fddeaea2d97bdab24235-3648-4c22-9999-82b2a146efef2021-10-12WarningsExact identifier
spl id: f5a14b59-3491-4585-a559-fddeaea2d97b
spl set id: dab24235-3648-4c22-9999-82b2a146efef

Reported adverse events (FAERS/openFDA)#

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