Label: DERMAHAN V10 WHITENING TONE UPCREAM- adenosine, niacinamide cream
- NDC Code(s): 82083-0014-1
- Packager: LAON COMMERCE co ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 March 6, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
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 - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
-
WARNINGS
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
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DERMAHAN V10 WHITENING TONE UPCREAM
adenosine, niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82083-0014 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:82083-0014-1 50 mL in 1 TUBE; Type 0: Not a Combination Product 03/07/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/07/2023 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(82083-0014) , label(82083-0014)
