DERMAHAN V10 WHITENING TONE UPCREAM- adenosine, niacinamide cream 
LAON COMMERCE co ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Adenosine, Niacinamide

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

whitening, wrinkle care

KEEP OUT OF REACH OF THE CHILDREN

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

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

topical use only

label

DERMAHAN V10 WHITENING TONE UPCREAM 
adenosine, niacinamide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82083-0014
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82083-0014-150 mL in 1 TUBE; Type 0: Not a Combination Product03/07/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/07/2023
Labeler - LAON COMMERCE co ltd (557839830)
Registrant - LAON COMMERCE co ltd (557839830)
Establishment
NameAddressID/FEIBusiness Operations
LAON COMMERCE CO Ltd557839830manufacture(82083-0014) , label(82083-0014)

Revised: 3/2023
Document Id: f644c802-85aa-73d4-e053-2a95a90ac4e6
Set id: f644b6bf-e511-196f-e053-2a95a90a13b1
Version: 1
Effective Time: 20230306
 
LAON COMMERCE co ltd