Label: INCELLDERM 4D LUSTRE CUSHION- titanium dioxide, ethylhexyl methoxycinnamate, ethylhexyl salicylate, niacinamide, adenosine powder
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Contains inactivated NDC Code(s)
NDC Code(s): 72650-070-01, 72650-070-02 - Packager: Riman 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 June 10, 2020
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Water, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Cyclohexasiloxane, Cyclopentasiloxane, Phenyl Trimethicone, 1,2-Hexanediol, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Octyldodecanol, Glycerin, Methylpropanediol, Triethylhexanoin, Polyisobutene, Cetyl Ethylhexanoate, Dimethicone, Caprylic/Capric Triglyceride, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sodium Chloride, Mica, Hydrogenated Polyisobutene, Ozokerite, Diphenylsiloxy Phenyl Trimethicone, Methyl Methacrylate Crosspolymer, CI 77492, Stearic Acid, Hyaluronic Acid, Aluminum Hydroxide, Beeswax, Disteardimonium Hectorite, Sorbitan Sesquioleate, Butyrospermum Parkii (Shea) Butter, CI 77491, Xanthan Gum, Fragrance, Polymethyl Methacrylate, Lactobacillus Ferment Lysate, Canola Oil, Propylene Carbonate, Tocopheryl Acetate, Maltodextrin, Saccharide Hydrolysate, Distarch Phosphate, CI 77499, Caprylyl Glycol, Ceramide NP, Anhydroxylitol, Xylitylglucoside, Triethoxycaprylylsilane, Phytosphingosine, Xylitol, Akebia Quinata Extract, Disodium EDTA, Zinc Oxide, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Lithospermum Erythrorhizon Root Extract, Ultramarines, Angelica Dahurica Root Extract, Angelica Gigas Root Extract, Citrus Unshiu Peel Extract, Pichia Anomala Extract, Prunus Armeniaca (Apricot) Kernel Extract, Sesamum Indicum (Sesame) Seed Extract, Xanthium Strumarium Fruit Extract, Centella Asiatica Extract, Daucus Carota Sativa (Carrot) Seed Oil, Hydrogen Dimethicone, Camellia Sinensis Leaf Extract, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Chenopodium Album Flower Extract, Corydalis Ochotensis Extract, Draba Nemorosa Extract, Lactuca Indica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Beta-Carotene, Daucus Carota Sativa (Carrot) Root Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Helianthus Annuus (Sunflower) Seed Oil, Centella Asiatica Extract, Aloe Barbadensis Leaf Extract, Lavandula Angustifolia (Lavender) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Pulsatilla Koreana Extract, Usnea Barbata (Lichen) Extract, Zanthoxylum Piperitum Fruit Extract, Ethylhexylglycerin
- PURPOSE
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WARNINGS
1. When or after using cosmetics, consult with a specialist, if you have abnormal symptoms such as red spot, swelling or itching or side effects due to direct sunlight.
2. Do not use in wounded areas.
3. Cautions for storage and handling a) Keep out of reach of children. b) Store away from direct sunlight. - KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- Questions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
INCELLDERM 4D LUSTRE CUSHION
titanium dioxide, ethylhexyl methoxycinnamate, ethylhexyl salicylate, niacinamide, adenosine powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72650-070 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium Dioxide 1.37 g in 15 g Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 1.05 g in 15 g Octisalate (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) Octisalate 0.72 g in 15 g Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.30 g in 15 g Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.006 g in 15 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72650-070-02 2 in 1 CARTON 06/01/2020 1 NDC:72650-070-01 15 g 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 06/01/2020 Labeler - Riman Co., Ltd. (694893735) Registrant - Riman Co., Ltd. (694893735) Establishment Name Address ID/FEI Business Operations ATEC Co., Ltd. 689276681 manufacture(72650-070)