Label: YSE BEAUTY SKIN GLOW SPF 30 PRIMER- avobenzone, homosalate, octisalate, octocrylene cream
- NDC Code(s): 84075-000-00
- Packager: MSS Beauty, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 31, 2024
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- Official Label (Printer Friendly)
- 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
- 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 of 15 or higher and other sun protection measures including:
- Limit time in the sun, especially from 10 a.m. - 2 p.m.
- Wear long-sleeve shirts, pants, hats, and sunglasses
- Children under 6 months: Ask a doctor
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Inactive ingredients
Water (Aqua), Propanediol, Butyloctyl Salicylate, Cetearyl Alcohol, Polymethylsilsesquioxane, Dimethicone, Dicaprylyl Carbonate, Bismuth Oxychloride (CI 77163), Glyceryl Stearate, Jojoba Esters, Sodium stearoyl Glutamate, Phenoxyethanol, Dimethicone Crosspolymer, Mica, Ethylhexyl Hydroxystearate, Xanthan Gum, Iron Oxides (CI 77491, CI 77492, CI 77499), ZHelianthus Annus (Sunflower) Seed Wax, Oryza Sativa (Rice) Bran Extract, Chlorphenesin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Caprylyl Glycol, Niacinamide, Titanium Dioxide (CI 77891), Ethylhexylglycerin Hexylene Glycol, Niacinamide, Titanium Dioxide (CI 77891), Ethylhexylglycerin Hexylene Glycol, Stearyl Glycyrrhetinate, Tetrasodium Glutamate Diacetate, Helianthus Annuus (Sunflower) Extract, Sucrose, Glycyrrhiza Glabra (Licorice) Root Extract, Sodium Hydroxide, Polyglycerin-3, Tocopherol, Rosmarinus Officinalis (Rosemary) Leaf Extract, Spirulina Maxima Extract, Sodium Hyaluronate, Lecithin.
- Other information
- Questions or comments
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INGREDIENTS AND APPEARANCE
YSE BEAUTY SKIN GLOW SPF 30 PRIMER
avobenzone, homosalate, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84075-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 60 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 75 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) PROPANEDIOL (UNII: 5965N8W85T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) DIMETHICONE (UNII: 92RU3N3Y1O) DICAPRYLYL CARBONATE (UNII: 609A3V1SUA) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) PHENOXYETHANOL (UNII: HIE492ZZ3T) MICA (UNII: V8A1AW0880) ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E) XANTHAN GUM (UNII: TTV12P4NEE) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV) RICE BRAN (UNII: R60QEP13IC) CHLORPHENESIN (UNII: I670DAL4SZ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) NIACINAMIDE (UNII: 25X51I8RD4) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP) SUCROSE (UNII: C151H8M554) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) SODIUM HYDROXIDE (UNII: 55X04QC32I) POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) TOCOPHEROL (UNII: R0ZB2556P8) ROSEMARY (UNII: IJ67X351P9) ARTHROSPIRA MAXIMA (UNII: 9K7IG15M0Q) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84075-000-00 1 in 1 CARTON 06/28/2023 1 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug OKM020 06/28/2023 Labeler - MSS Beauty, LLC (119146189)