DERMAHAN V10 WHITENING TONE UpCREAM

Manufacturer: LAON COMMERCE co ltd
Effective date: 2023-03-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:54:24

Label at a glance#

ProductDERMAHAN V10 WHITENING 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
Glycerin
Dimethicone
Titanium Dioxide
Cyclopentasiloxane
Panthenol
Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer
Trisiloxane
Dicaprylyl Carbonate
Isohexadecane
Dimethiconol
Silica
Sodium Polyacrylate
Benzyl Glycol
Ethylhexyl Stearate
Polysorbate 80
Ethylhexylglycerin
Triethoxycaprylylsilane
Aluminum Hydroxide
Allantoin
Trideceth-6
Citrus Aurantium Dulcis (Orange) Peel Oil
Sorbitan Oleate
Disodium EDTA
C11-13 Isoalkane
Litsea Cubeba Fruit Oil
Hydrogenated Lecithin
Polyglyceryl-10 Stearate
Tocopheryl Acetate
Sodium Ascorbyl Phosphate
Glyceryl Arachidonate
Glyceryl Linolenate
Pyridoxine
Folic Acid
Thiamine HCl
Biotin
Retinyl Palmitate
Cyanocobalamin
Limonene
Citral

OTC - PURPOSE SECTION

whitening, wrinkle care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Take an appropriate amount of this product and spread it evenly on the skin

WARNINGS SECTION

1. Consult a specialist, if there are abnormal symptoms or side effects such us red spots, swelling, or itching in the area of use due to direct sunlight when using or after using cosmetics.

2. Refrain from using on area s with wounds.

3. Precaution for storage and handling a) Keep out of reach of children b) Store away from direct sunlight

DOSAGE & ADMINISTRATION SECTION

topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
ADENOSINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
d676a241-be05-4740-b3ee-1a5f2ed422d2	Product name	4	20180615
dd8bd48f-20d6-43c7-b471-3ae872868afa	Product name	3	20180125
d41954ff-bc63-4b2c-aba0-9146707659d7	Product name	2	20151117

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82083-0014-1	DERMAHAN V10 WHITENING TONE UpCREAM	50 mL in 1 TUBE	CREAM	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82083-0014	DERMAHAN V10 WHITENING TONE UPCREAM (ADENOSINE, NIACINAMIDE) CREAM [LAON COMMERCE CO LTD]	1	Current NDC, 1 package rows	20230308_f644b6bf-e511-196f-e053-2a95a90a13b1.zip

Products#

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

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

DERMAHAN V10 WHITENING TONE UpCREAM
adenosine, niacinamide
WATER
ADENOSINE
NIACINAMIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82083-0014	82083-0014-1

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ADENOSINE	K72T3FS567	ACTIB
NIACINAMIDE	25X51I8RD4	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DERMAHAN V10 WHITENING TONE UpCREAM	ADENOSINE, NIACINAMIDE	LAON COMMERCE co ltd	f644b6bf-e511-196f-e053-2a95a90a13b1	2023-03-06	Warnings	Exact identifier ndc (package): 82083-0014-1 ndc (product): 82083-0014 ndc11 (package): 82083001401 spl id: f644c802-85aa-73d4-e053-2a95a90ac4e6 spl set id: f644b6bf-e511-196f-e053-2a95a90a13b1

Reported adverse events (FAERS/openFDA)#

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