Label: LUPIUM MOISTURE WATER SUN SERUM- niacinamide, titanium dioxide, adenosine, zinc oxide liquid
-
Contains inactivated NDC Code(s)
NDC Code(s): 82284-010-01, 82284-010-02 - Packager: JYOONCOSMETICS 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 October 12, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
-
INACTIVE INGREDIENTS
Water, Dibutyl Adipate, Phenethyl Benzoate, Butylene Glycol, Butyloctyl Salicylate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Diphenylsiloxy Phenyl Trimethicone, Polysilicone-15, Alcohol, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Ethylhexyl Triazone, Diethylhexyl Butamido Triazone, C12-15 Alkyl Benzoate, 1,2-Hexanediol, Pentylene Glycol, Sodium Acrylates Crosspolymer-2, C14-22 Alcohols, C20-22 Alkyl Phosphate, Polyglyceryl-3 Distearate, C20-22 Alcohols, Decyl Glucoside, Hydroxyacetophenone, Potassium Cetyl Phosphate, Silica, C12-20 Alkyl Glucoside, Tromethamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aluminum Hydroxide, Fragrance(Parfum), Glycerin, Glyceryl Stearate Citrate, Sodium Phytate, Isostearic Acid, Polyhydroxystearic Acid, Xanthan Gum, Squalane, Sodium Hyaluronate, Glyceryl Caprylate, Ceramide NP, Hydroxypropyltrimonium Hyaluronate, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronate, Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Potassium Hyaluronate, rh-Oligopeptide-1, rh-Oligopeptide-2, rh-Polypeptide-1
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LUPIUM MOISTURE WATER SUN SERUM
niacinamide, titanium dioxide, adenosine, zinc oxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82284-010 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 Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.005 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:82284-010-02 1 in 1 CARTON 10/01/2021 1 NDC:82284-010-01 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 Cosmax, Inc. 689049693 manufacture(82284-010)
