Label: DERMABLEND PROFESSIONAL CC CONTINUOUS CORRECTION FULL COVERAGE MAKEUP BROAD SPECTRUM SPF 50 PLUS SUNSCREEN- homosalate, octisalate and octocrylene cream
- NDC Code(s): 49967-451-01
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 27, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Flammable until dry.
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
For sunscreen 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:
● 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
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Inactive ingredients
water, dimethicone, propanediol, alcohol denat., synthetic fluorphlogopite, niacinamide, vinyl dimethicone/methicone silsesquioxane crosspolymer, caffeine, tocopherol, scutellaria baicalensis root extract, PEG-30 dipolyhydroxystearate, aluminum hydroxide, magnesium sulfate, disodium stearoyl glutamate, disteardimonium hectorite, polyglyceryl-4 diisostearate/polyhydroxystearate/sebacate, phenoxyethanol, may contain: titanium dioxide, iron oxides
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INGREDIENTS AND APPEARANCE
DERMABLEND PROFESSIONAL CC CONTINUOUS CORRECTION FULL COVERAGE MAKEUP BROAD SPECTRUM SPF 50 PLUS SUNSCREEN
homosalate, octisalate and octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-451 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 100 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 49 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) PROPANEDIOL (UNII: 5965N8W85T) ALCOHOL (UNII: 3K9958V90M) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) NIACINAMIDE (UNII: 25X51I8RD4) VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR) CAFFEINE (UNII: 3G6A5W338E) TOCOPHEROL (UNII: R0ZB2556P8) SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S) PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) PHENOXYETHANOL (UNII: HIE492ZZ3T) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-451-01 1 in 1 CARTON 08/20/2021 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 08/20/2021 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA Products, Inc. 624244349 manufacture(49967-451) , pack(49967-451)
