Tenue Whitenning Tone upCream

Manufacturer
LAON COMMERCE co ltd
Effective date
2022-10-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:51:15

Label at a glance#

ProductTenue Whitenning Tone upCream
Active ingredientADENOSINE, NIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Adenosine, Niacinamide

INACTIVE INGREDIENT SECTION

Water
Butylene Glycol
Cyclopentasiloxane
Glycerin
Glycereth-26
Isoamyl Laurate
1,2-Hexanediol
Cetyl Ethylhexanoate
Caprylic/Capric Triglyceride
Niacinamide
Titanium Dioxide
Cyclohexasiloxane
Butylene Glycol Dicaprylate/Dicaprate
Polysorbate 60
Betaine
Prunus Amygdalus Dulcis (Sweet Almond) Oil
Butyrospermum Parkii (Shea Butter)
Polyacrylamide
Dimethiconol
Arginine
Carbomer
C13-14 Isoparaffin
Malpighia Emarginata (Acerola) Fruit Extract
Portulaca Oleracea Extract
Nelumbo Nucifera Flower Extract
Rosmarinus Officinalis (Rosemary) Leaf Extract
Chamomilla Recutita (Matricaria) Flower Extract
Olea Europaea (Olive) Fruit Extract
Melaleuca Alternifolia (Tea Tree) Extract
Tremella Fuciformis (Mushroom) Extract
Centella Asiatica Extract
Salvia Officinalis (Sage) Leaf Extract
Salix Alba (Willow) Bark Extract
Aluminum Hydroxide
Laureth-7
Allantoin
Adenosine
Disodium EDTA
Dipotassium Glycyrrhizate
Sodium Hyaluronate
Fragrance
Triethoxycaprylylsilane
Ethylhexylglycerin

OTC - PURPOSE SECTION

whitening, wrinkle care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

At the last step of skincare, take an appropriate amount and spread it all over your face and absorb it

WARNINGS SECTION

1. consult a specialist if there are any abnormal symptoms or side effects such as red spots, swelling, or itching due to direct sunlight when using cosmetics

2. avoid using them in areas with wounds

3. precautions for storage and handling

a) keep out of reach of childrea

b) keep away from direct sunlight

DOSAGE & ADMINISTRATION SECTION

topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82083-0013-1Tenue Whitenning Tone upCream50 mL in 1 TUBECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82083-0013TENUE WHITENNING TONE UPCREAM (ADENOSINE, NIACINAMIDE) CREAM [LAON COMMERCE CO LTD]1Current NDC, Legacy NDC, 1 package rows20221029_ebf955a9-31af-b13b-e053-2a95a90a4d3b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82083-001382083-0013-1

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
WATER059QF0KO0RIACT
ADENOSINEK72T3FS567ACTIB
NIACINAMIDE25X51I8RD4ACTIB

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
Tenue Whitenning Tone upCreamADENOSINE, NIACINAMIDELAON COMMERCE co ltdebf955a9-31af-b13b-e053-2a95a90a4d3b2022-10-26WarningsExact identifier
ndc (package): 82083-0013-1
ndc (product): 82083-0013
ndc11 (package): 82083001301
spl id: ebf95552-db2f-bd6f-e053-2a95a90a8857
spl set id: ebf955a9-31af-b13b-e053-2a95a90a4d3b

Reported adverse events (FAERS/openFDA)#

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