Label: DERMAHAN UV SUN- adenosine, niacinamide cream
- NDC Code(s): 82083-0016-1
- Packager: LAON COMMERCE co ltd
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated April 17, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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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
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DERMAHAN UV SUN
adenosine, niacinamide creamProduct 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)
