Label: GLOW RADIANT MOISTURIZER SPF 15- octinoxate, octocrylene, octisalate, oxybenzone, avobenzone cream
- NDC Code(s): 76354-650-01
- Packager: e.l.f. Cosmetics, Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 12, 2024
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- Drug Facts
- Active Ingredients
- Uses
- Warnings
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Directions
• apply liberally 15 minutes before sun exposure. • reapply at least every 2 hours. • use a water resistant sunscreen if swimming or sweating. • Spending time in the sun increases your risk of sun 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: For sunscreen use:Sun Protection Measures:
• limit time in the sun, especially from 10 a.m.-2 p.m.
• wear long-sleeved shirts, pants, hats and sunglasses
• children under 6 months of age: Ask a doctor.
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Inactive Ingredients
Water (Aqua), Butylene Glycol, C12-15 Alkyl Benzoate, Glycerin, Glyceryl Stearate, PEG-100 Stearate, Mica, Cetearyl Olivate, Cyclopentasiloxane, Sorbitan Olivate, Stearic Acid, Cetearyl Alcohol, Dimethicone, Tocopheryl Acetate (Ve), Cocos Nucifera (Coconut) Oil, Butyrospermum Parkii (Shea Butter), Hydrolyzed Hyaluronic Acid, Phenoxyethanol, Caprylyl Glycol, Acrylates/Polytrimethylsiloxymethacrylate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tromethamine, Fragrance (Parfum), Disodium EDTA, Bisabolol, Synthetic Fluorphlogopite, Silica, Tin Oxide, MAY CONTAIN: Titanium Dioxide (CI 77891), Red 40 (CI 16035), Yellow 5 (CI 19140)
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INGREDIENTS AND APPEARANCE
GLOW RADIANT MOISTURIZER SPF 15
octinoxate, octocrylene, octisalate, oxybenzone, avobenzone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76354-650 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 71 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 38 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 45 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 28 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 25 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) PEG-100 STEARATE (UNII: YD01N1999R) MICA (UNII: V8A1AW0880) CETEARYL OLIVATE (UNII: 58B69Q84JO) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) SORBITAN OLIVATE (UNII: MDL271E3GR) STEARIC ACID (UNII: 4ELV7Z65AP) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N) COCONUT OIL (UNII: Q9L0O73W7L) SHEA BUTTER (UNII: K49155WL9Y) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TROMETHAMINE (UNII: 023C2WHX2V) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) LEVOMENOL (UNII: 24WE03BX2T) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) STANNIC OXIDE (UNII: KM7N50LOS6) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76354-650-01 36 mL in 1 BOTTLE; Type 0: Not a Combination Product 10/01/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/01/2018 12/12/2024 Labeler - e.l.f. Cosmetics, Inc (093902816) Establishment Name Address ID/FEI Business Operations Zhejiang Ayan Biotech Co.,Ltd. 544377996 manufacture(76354-650)
