Label: NYX PROFESSIONAL MAKEUP BUTTERMELT GLAZE SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30- homosalate,octisalate and octocrylene cream
- NDC Code(s): 49967-356-01
- Packager: L’Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 23, 2024
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
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
Directions
For sunscreen use:
- shake well before use
- 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 value of 15 or higher and other sun protection measures including:
o wear long-sleeved shirts, pants, hats, and sunglasses
- children under 6 months of age: Ask a doctor
- Other information
-
Inactive ingredients
water, glycerin, caprylyl methicone, dimethicone, silica, butyloctyl salicylate, cetyl PEG/PPG-10/1 dimethicone, niacinamide, propanediol, dimethicone/PEG-10/15 crosspolymer, camellia sinensis leaf extract, mangifera indica (mango) seed butter, butyrospermum parkii (shea) butter, simethicone, sodium chloride, sodium citrate, sodium hyaluronate, silica silylate, trimethylsiloxysilicate, aluminum hydroxide, adenosine, disodium stearoyl glutamate, dipropylene glycol, caprylyl glycol, citric acid, trisodium ethylenediamine disuccinate, maltodextrin, synthetic fluorphlogopite, disteardimonium hectorite, tocopherol, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, phenoxyethanol, chlorphenesin, fragrance, limonene; may contain: titanium dioxide, iron oxides
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NYX PROFESSIONAL MAKEUP BUTTERMELT GLAZE SOFT GLOW SKIN TINT SUNSCREEN BROAD SPECTRUM SPF 30
homosalate,octisalate and octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-356 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 73 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (ETHYLHEXYL SALICYLATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 60 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CAPRYLYL METHICONE (UNII: Q95M2P1KJL) DIMETHICONE (UNII: 92RU3N3Y1O) SILICA (UNII: ETJ7Z6XBU4) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) NIACINAMIDE (UNII: 25X51I8RD4) PROPANEDIOL (UNII: 5965N8W85T) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) CAMELLIA SINENSIS LEAF (UNII: W2ZU1RY8B0) MANGIFERA INDICA (MANGO) SEED BUTTER (UNII: 4OXD9M35X2) BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM CITRATE (UNII: 1Q73Q2JULR) SODIUM HYALURONATE (UNII: YSE9PPT4TH) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) ADENOSINE (UNII: K72T3FS567) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) DIPROPYLENE GLYCOL (UNII: E107L85C40) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CITRIC ACID (UNII: 2968PHW8QP) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) MALTODEXTRIN (UNII: 7CVR7L4A2D) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) TOCOPHEROL (UNII: R0ZB2556P8) PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) LIMONENE, (+)- (UNII: GFD7C86Q1W) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) IRON OXIDES (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-356-01 1 in 1 CARTON 01/10/2024 1 30 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/10/2024 Labeler - L’Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations Beauty Manufacturing Solutions Corp. 783200723 manufacture(49967-356)


