DERMAHAN UV SUN- adenosine, niacinamide cream

DERMAHAN UV SUN by

Drug Labeling and Warnings

DERMAHAN UV SUN by is a Otc medication manufactured, distributed, or labeled by LAON COMMERCE co ltd, LAON COMMERCE CO Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Niacinamide, Adenosine

INACTIVE INGREDIENT

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

PURPOSE

skin protect

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

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

WARNINGS

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.

DOSAGE & ADMINISTRATION

topical use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DERMAHAN UV SUN 
adenosine, niacinamide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82083-0016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567)	ADENOSINE	0.04 g  in 100 mL
NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4)	NIACINAMIDE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82083-0016-1	50 mL in 1 TUBE; Type 0: Not a Combination Product	04/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/01/2023

Labeler - LAON COMMERCE co ltd (557839830)

Registrant - LAON COMMERCE co ltd (557839830)

Establishment
Name	Address	ID/FEI	Business Operations
LAON COMMERCE CO Ltd		557839830	manufacture(82083-0016) , label(82083-0016)