Label: REOGANIC EX WHITENING PORE CARE DEODORANT- arbutin, niacinamide, adenosine liquid
- NDC Code(s): 82083-0025-1
- 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 September 22, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Water
Alcohol Denat
Dipropylene Glycol
1,2-Hexanediol
PEG-60 Hydrogenated Castor Oil
Methyl Diisopropyl Propionamide
Silica
Caprylyl Glycol
Carbomer
Tromethamine
Allantoin
Ethylhexylglycerin
Disodium EDTA
Rosmarinus Officinalis (Rosemary) Leaf Extract
Chamomilla Recutita (Matricaria) Flower Extract
Centella Asiatica Extract
Salvia Officinalis (Sage) Leaf Extract
Portulaca Oleracea Extract
Nelumbo Nucifera Flower Extract
Olea Europaea (Olive) Fruit Extract
Melaleuca Alternifolia (Tea Tree) Extract
Tremella Fuciformis (Mushroom) Extract
Salix Alba (Willow) Bark Extract
Glycerin
Butylene Glycol
Sodium Hyaluronate
Glutathione
Fragrance
Benzyl Salicylate
Coumarin
Limonene
Linalool - PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
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WARNINGS
[Precautions for use]
1. During using product or after use, if there are any abnormal symptoms or side effects such as red spots, swelling, or itching on the area of use due to direct sunlight, con sult with a specialist. 2. Refrain from using on areas with scars, etc. 3. Pre cautions for storage and handling A) Keep out of reach of children B) Store away from direct sunlight 4. For arbutin, papules and mild itching have been repo rted in 「Human Application Test Data」.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
REOGANIC EX WHITENING PORE CARE DEODORANT
arbutin, niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82083-0025 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 5 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL ARBUTIN (UNII: C5INA23HXF) (ARBUTIN - UNII:C5INA23HXF) ARBUTIN 5 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82083-0025-1 60 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 09/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2023 Labeler - LAON COMMERCE co ltd (557839830) Registrant - LAON COMMERCE co ltd (557839830) Establishment Name Address ID/FEI Business Operations LAON COMMERCE CO Ltd 557839830 label(82083-0025) , manufacture(82083-0025)
