DERMAHAN UV SUN- 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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Niacinamide, Adenosine

Water
Zinc Oxide
Cyclopentasiloxane
Titanium Dioxide
Butyloctyl Salicylate
Glycerin
Cetyl PEG/PPG-10/1 Dimethicone
Niacinamide
Dicaprylyl Carbonate
Sodium Chloride
Triethoxycaprylylsilane
Aluminum Hydroxide Oxide
PEG-10 Dimethicone
Panthenol
Stearic Acid
Disteardimonium Hectorite
Benzyl Glycol
Water
Styrene/Acrylates Copolymer
Butylene Glycol
Allantoin
Propylene Carbonate
Ethylhexylglycerin
Adenosine
Disodium EDTA
1,2-Hexanediol
Borago Officinalis Extract
Corchorus Olitorius Leaf Extract
Ilex Paraguariensis Leaf Extract
Daucus Carota Sativa (Carrot) Root Extract
Sodium Hyaluronate
Fragrance

skin protect

KEEP OUT OF REACH OF THE CHILDREN

In the last step of basic care, apply an appropriate amount to the face, neck, arms, legs, etc. that are prone to UV exposure.

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

2. Refrain from using it on injured areas, etc.

3. Precautions for storage and handling A) Keep it out of reach of children. B) Keep away from direct sunlight

3. Protects the skin from UV rays(SPF50+/PA++++) Helps whiten the skin. It helps to improve wrinkles on the skin.

topical use only

1

DERMAHAN UV SUN 
adenosine, niacinamide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82083-0016
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:82083-0016-150 mL in 1 TUBE; Type 0: Not a Combination Product04/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/01/2023
Labeler - LAON COMMERCE co ltd (557839830)
Registrant - LAON COMMERCE co ltd (557839830)
Establishment
NameAddressID/FEIBusiness Operations
LAON COMMERCE CO Ltd557839830manufacture(82083-0016) , label(82083-0016)

Revised: 4/2023
Document Id: f992b41b-850a-37e1-e053-6294a90adb4b
Set id: f992b41b-850b-37e1-e053-6294a90adb4b
Version: 1
Effective Time: 20230417
 
LAON COMMERCE co ltd