Label: PURPLEU GLOW TONE IT LIKE SNOW- dimethicone, titanium dioxide, niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 90069-203-01 - Packager: Purple U Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 2, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Stop use and ask a doctor if
- Keep out of reach of children
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Directions
- Apply liberally 15 minutes before sun exposure
- Reapply at least every 2 hours
- Use water resistant sunscreen if swimming or sweating
- Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with a Broad-Spectrum SPF value of 15 or higher and other sun protection measures including:
- Limit time in sun, especially from 10a.m.–2 p.m.
- Wear long-sleeved shirts, pants, hats, and sunglasses
- Children under 6 months: ask a doctor
- Other information
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Inactive ingredients
Water, Ethylhexyl Methoxycinnamate, Cyclopentasiloxane, Butylene Glycol, Glycerin, Titanium Dioxide (CI 77891), Ethylhexyl Salicylate, Pentylene Glycol,C12-15 Alkyl Benzoate, Cetyl Ethylhexanoate, Niacinamide, Dicaprylyl Carbonate, Mica (CI 77019), Adansonia Digitata Fruit Extract, Pelargonium Graveolens Flower Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Rosa Damascena Flower Water, Hippophae Rhamnoides Fruit Extract, Sodium Hyaluronate, Nelumbo Nucifera Flower Extract, Nymphaea Alba Flower Extract, Prunus Serrulata Flower Extract, Rosa Hybrid Flower Extract, Hydrolyzed Hyaluronic Acid, Hyaluronic Acid, Raspberry Ketone, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Polysorbate 60, Triceteareth-4 Phosphate, Glycol Stearate, Caprylyl Methicone, Acrylates/ C10-30 Alkyl Acrylate Crosspolymer, Glyceryl Stearate, PEG-100 Stearate, Potassium Cetyl Phosphate, Silica, Dimethicone, Tromethamine, PEG-2 Stearate, Lactose, Aluminum Hydroxide, PEG-10 Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Cellulose, Stearic Acid, Isohexadecane, Ethylhexylglycerin,Triethoxycaprylylsilane, Adenosine, Polysorbate 80, Hydroxypropyl Methylcellulose, Tocopheryl Acetate, Sorbitan Oleate, Glutathione, Caprylic/Capric Triglyceride, Propanediol, Tocopherol, Hydrogenated Lecithin, Sodium Hyaluronate Crosspolymer, Hydrolyzed Glycosaminoglycans, Ceramide NP, Benzyl Glycol, 1,2-Hexanediol, Caprylyl Glycol, Octanediol, Disodium EDTA, Phenoxyethanol, Potassium Sorbate, Fragrance(Parfum), Iron Oxides(CI 77491)
- Package Label
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INGREDIENTS AND APPEARANCE
PURPLEU GLOW TONE IT LIKE SNOW
dimethicone, titanium dioxide, niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:90069-203 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 0.04 g in 100 mL DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 0.45 g in 100 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 2.94 g in 100 mL NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TROMETHAMINE (UNII: 023C2WHX2V) PEG-2 STEARATE (UNII: 94YQ11Y95F) LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) POWDERED CELLULOSE (UNII: SMD1X3XO9M) STEARIC ACID (UNII: 4ELV7Z65AP) ISOHEXADECANE (UNII: 918X1OUF1E) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) OCTINOXATE (UNII: 4Y5P7MUD51) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) GLYCERIN (UNII: PDC6A3C0OX) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) POLYSORBATE 80 (UNII: 6OZP39ZG8H) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) SORBITAN MONOOLEATE (UNII: 06XEA2VD56) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) TOCOPHEROL (UNII: R0ZB2556P8) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T) NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O) PRUNUS SERRULATA FLOWER (UNII: 60I4615G0K) 4-(P-HYDROXYPHENYL)-2-BUTANONE (UNII: 7QY1MH15BG) POLYSORBATE 60 (UNII: CAL22UVI4M) GLYCOL STEARATE (UNII: 0324G66D0E) PEG-100 STEARATE (UNII: YD01N1999R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20) TRICETEARETH-4 PHOSPHATE (UNII: 69534Y66NO) JOJOBA OIL (UNII: 724GKU717M) PROPANEDIOL (UNII: 5965N8W85T) ETHYLENE GLYCOL MONOBENZYL ETHER (UNII: 06S8147L47) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ROSA DAMASCENA FLOWER OIL (UNII: 18920M3T13) NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV) GLUTATHIONE (UNII: GAN16C9B8O) HYDROLYZED GLYCOSAMINOGLYCANS (BOVINE; 50000 MW) (UNII: 997385V0VV) CERAMIDE NP (UNII: 4370DF050B) CAPRYLYL GLYCOL (UNII: 00YIU5438U) OCTANEDIOL (UNII: 806K32R50Z) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PHENOXYETHANOL (UNII: HIE492ZZ3T) FERRIC OXIDE RED (UNII: 1K09F3G675) WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) OCTISALATE (UNII: 4X49Y0596W) MICA (UNII: V8A1AW0880) ADANSONIA DIGITATA FRUIT (UNII: 51N9TR1W6P) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PENTYLENE GLYCOL (UNII: 50C1307PZG) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) CETYL ETHYLHEXANOATE (UNII: 134647WMX4) HYALURONATE SODIUM (UNII: YSE9PPT4TH) HYALURONIC ACID (UNII: S270N0TRQY) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:90069-203-01 35 mL in 1 BOTTLE; Type 0: Not a Combination Product 09/02/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/02/2020 Labeler - Purple U Co., Ltd (694823532) Registrant - RECIPE CO., LTD (631158768) Establishment Name Address ID/FEI Business Operations RECIPE CO., LTD 631158768 manufacture(90069-203)