Label: IT COSMETICS YOUR SKIN BUT BETTER CC PLUS NUDE GLOW COLOR CORRECTING MEDIUM COVERAGE SKIN TINT PLUS BRIGHTENING GLOW SERUM PLUS BROAD SPECTRUM SPF 40 SUNSCREEN- homosalate, octisalate and octocrylene liquid
- NDC Code(s): 49967-964-01
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 28, 2024
If you are a consumer or patient please visit this version.
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- 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:
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant susncreen if swiming 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 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
- Other information
-
Inactive ingredients
water, glycerin, caprylyl methicone, dimethicone, butyloctyl salicylate, cetyl PEG/PPG-10 dimethicone, niacinamide, propanediol, dimethicone/PEG-10/15 crosspolymer, synthetic fluorphlogopite, phenoxyethanol, sodium chloride
trimethylsiloxysilicate, disteardimonium hectorite, disodium stearoyl glutamate, fragrance, chlorphenesin, caprylyl glycol, silica silylate, trisodium ethylenediamine disuccinate, limonene, simethicone, maltodextrin, aluminum hydroxide, adenosine, dipropylene glycol, sodium hyaluronate, citral, citric acid, linalool, sodium citrate, camellia sinensis leaf extract, tocopherol, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate; may contain: titanium dioxide, iron oxides - Questions or comments?
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INGREDIENTS AND APPEARANCE
IT COSMETICS YOUR SKIN BUT BETTER CC PLUS NUDE GLOW COLOR CORRECTING MEDIUM COVERAGE SKIN TINT PLUS BRIGHTENING GLOW SERUM PLUS BROAD SPECTRUM SPF 40 SUNSCREEN
homosalate, octisalate and octocrylene liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-964 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) (OCTISALATE - 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 TRISILOXANE (UNII: Q95M2P1KJL) DIMETHICONE (UNII: 92RU3N3Y1O) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) NIACINAMIDE (UNII: 25X51I8RD4) PROPANEDIOL (UNII: 5965N8W85T) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM CHLORIDE (UNII: 451W47IQ8X) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) CHLORPHENESIN (UNII: I670DAL4SZ) CAPRYLYL GLYCOL (UNII: 00YIU5438U) TRISODIUM ETHYLENEDIAMINE DISUCCINATE (UNII: YA22H34H9Q) LIMONENE, (+)- (UNII: GFD7C86Q1W) MALTODEXTRIN (UNII: 7CVR7L4A2D) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) ADENOSINE (UNII: K72T3FS567) DIPROPYLENE GLYCOL (UNII: E107L85C40) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CITRAL (UNII: T7EU0O9VPP) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) LINALOOL, (+/-)- (UNII: D81QY6I88E) SODIUM CITRATE (UNII: 1Q73Q2JULR) GREEN TEA LEAF (UNII: W2ZU1RY8B0) TOCOPHEROL (UNII: R0ZB2556P8) PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-964-01 1 in 1 CARTON 08/01/2024 1 32 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 08/01/2024 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations Beauty Manufacturing Solutions Corp. 783200723 manufacture(49967-964)
