Label: LUPIUM MOISTURE TONE UP SUN SERUM- niacinamide, titanium dioxide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82284-020-01, 82284-020-02 - Packager: JYOONCOSMETICS Co, Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated October 12, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
WATER, DIBUTYL ADIPATE, PROPANEDIOL, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, POLYMETHYLSILSESQUIOXANE, BUTYLENE GLYCOL, ETHYLHEXYL TRIAZONE, METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL, COCO-CAPRYLATE/CAPRATE, CAPRYLYL METHICONE, DIETHYLHEXYL BUTAMIDO TRIAZONE, GLYCERIN, 1,2-HEXANEDIOL, PANCRATIUM MARITIMUM EXTRACT, HIBISCUS SABDARIFFA FLOWER EXTRACT, PENTYLENE GLYCOL, BEHENYL ALCOHOL, POLY C10-30 ALKYL ACRYLATE, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, DECYL GLUCOSIDE, TROMETHAMINE, CARBOMER, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, SODIUM STEAROYL GLUTAMATE, POLYACRYLATE CROSSPOLYMER-6, ETHYLHEXYLGLYCERIN, XANTHAN GUM, t-BUTYL ALCOHOL, TOCOPHEROL, TREHALOSE, GLUTATHIONE, BISABOLOL, TRANEXAMIC ACID, GLYCERYL POLYMETHACRYLATE, BETA-GLUCAN, PROPYLENE GLYCOL, PALMITOYL TRIPEPTIDE-1, FRAGRANCE, IRON OXIDES(CI 77491)
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LUPIUM MOISTURE TONE UP SUN SERUM
niacinamide, titanium dioxide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82284-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.00 g in 50 mL Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium Dioxide 0.86 g in 50 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.02 g in 50 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Dibutyl Adipate (UNII: F4K100DXP3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82284-020-02 1 in 1 CARTON 10/01/2021 1 NDC:82284-020-01 50 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 10/01/2021 Labeler - JYOONCOSMETICS Co, Ltd (694915763) Registrant - JYOONCOSMETICS Co, Ltd (694915763) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co.,LTD. Gwanjeong Factory 689512611 manufacture(82284-020)