Label: SISEUNDEUSI LUMINANT- niacinamide, adenosine emulsion
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Contains inactivated NDC Code(s)
NDC Code(s): 70098-0006-1 - Packager: GK COSMETIC 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 February 6, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Aloe Barbadensis Leaf Water, Glycerin, Butylene Glycol, Houttuynia Cordata Extract, Perilla Frutescens Leaf Extract, 1,2-Hexanediol, Acanthopanax Senticosus (Eleuthero) Root Extract, Camellia Sinensis Leaf Extract, Portulaca Oleracea Extract, Spirodela Polyrrhiza Extract, Phellinus Linteus Extract, Ganoderma Lucidum (Mushroom) Extract, Picrasma Excelsa Wood Extract, Nelumbium Speciosum Flower Extract, Cetearyl Alcohol, Sodium Hyaluronate, Cetyl Ethylhexanoate, Glyceryl Stearate, Stearic Acid, Sorbitan Stearate, Phytosqualane, Argania Spinosa Kernel Oil, Arginine , Carbomer, Citrus Limon (Lemon) Fruit Oil, Cyclopentasiloxane, Cyclohexasiloxane, Disodium EDTA, Xanthan Gum, Bletilla Striata Root Extract, Carthamus Tinctorius (Safflower) Flower Extract, Ganoderma Lucidum (Mushroom) Stem Extract, Ginkgo Biloba Leaf Extract, Glycine Soja (Soybean) Seed Extract, Magnolia Obovata Bark Extract, Oryza Sativa (Rice) Bran Extract, Phellodendron Amurense Bark Extract, Pinus Densiflora Extract, Polygonum Cuspidatum Root Extract, Polygonum Fagopyrum Seed Extract, Poria Cocos Extract, Prunus Armeniaca (Apricot) Kernel Extract, Prunus Mume Fruit Extract, Rehmannia Glutinosa Root Extract, Sanguisorba Officinalis Root Extract, Saururus Chinensis Leaf/Root Extract, Schizonepeta Tenuifolia Extract, Sophora Angustifolia Root Extract, Ulmus Davidiana Root Extract, Zanthoxylum Piperitum Fruit Extract
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
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WARNINGS
1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SISEUNDEUSI LUMINANT
niacinamide, adenosine emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70098-0006 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL Inactive Ingredients Ingredient Name Strength BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70098-0006-1 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/06/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/06/2017 Labeler - GK COSMETIC CO., LTD. (688477309) Registrant - GK COSMETIC CO., LTD. (688477309) Establishment Name Address ID/FEI Business Operations GK COSMETIC CO., LTD. 688477309 manufacture(70098-0006) , label(70098-0006) , pack(70098-0006)
