Label: INTENSITE CREME LUSTRE DAY SPF 30 US- avobenzone, octisalate, octocrylene cream
- NDC Code(s): 82691-142-00, 82691-142-01
- Packager: RV Skincare LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 6, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredients
- Uses
- Warnings
-
Directions
• For sunscreen use: • apply liberally 15 minutes before sun exposure • use a water resistant sunscreen if swimming or sweating • reapply at least every 2 hours • 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
Sun Protection Measures. - Other information
-
Inactive ingredients:
Aqua (Water, Eau), Helianthus Annuus (Sunflower) Seed Oil, Cyclopentasiloxane, Undecylcrylene Dimethicone, Butyloctyl Salicylate, Butylene Glycol, Cetearyl Alcohol, C13-15 Alkane, Glycerin, Sorbitan Stearate, PPG-2 Myristyl Ether Propionate, Potassium Cetyl Phosphate, Oligopeptide-20, Palmitoyl Tripeptide-1, Palmitoyl Tetrapeptide-7, Tocopheryl Acetate, Panthenol, Allantoin, Magnesium Ascorbyl Phosphate, Tocopherol, Chlorella Vulgaris Extract, Caprylyl Glycol, Sodium Oleate, Glycine Soja (Soybean) Oil, Hydrogenated Phosphatidylcholine, Cellulose Gum, Sodium Lactate, Mica, Dimethiconol, Lecithin, Polymethyl Methacrylate, Microcrystalline Cellulose, Aminomethyl Propanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Polysorbate 60, Parfum (Fragrance), Carbomer, Polysorbate 20, Sodium PCA, Phenoxyethanol, Citric Acid, Chlorphenesin, Disodium EDTA, Cyclohexasiloxane, Linalool, Citronellol, Limonene, Hexyl Cinnamal, CI 77891 (Titanium Dioxide).
- Questions or comments?
- Package Labeling:
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
INTENSITE CREME LUSTRE DAY SPF 30 US
avobenzone, octisalate, octocrylene creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82691-142 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 OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 80 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) SUNFLOWER OIL (UNII: 3W1JG795YI) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) UNDECYLCRYLENE DIMETHICONE (10000 MW) (UNII: HA26P2LA4P) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) C13-15 ALKANE (UNII: 114P5I43UJ) GLYCERIN (UNII: PDC6A3C0OX) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) PALMITOYL TRIPEPTIDE-1 (UNII: RV743D216M) PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) PANTHENOL (UNII: WV9CM0O67Z) ALLANTOIN (UNII: 344S277G0Z) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) TOCOPHEROL (UNII: R0ZB2556P8) CHLORELLA VULGARIS (UNII: RYQ4R60M02) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM OLEATE (UNII: 399SL044HN) SOYBEAN OIL (UNII: 241ATL177A) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SODIUM LACTATE (UNII: TU7HW0W0QT) MICA (UNII: V8A1AW0880) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) POLYSORBATE 60 (UNII: CAL22UVI4M) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) POLYSORBATE 20 (UNII: 7T1F30V5YH) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CHLORPHENESIN (UNII: I670DAL4SZ) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) CYCLOMETHICONE 6 (UNII: XHK3U310BA) LINALOOL, (+/-)- (UNII: D81QY6I88E) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) LIMONENE, (+)- (UNII: GFD7C86Q1W) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82691-142-00 1 in 1 CARTON 12/01/2017 1 50 mL in 1 JAR; Type 0: Not a Combination Product 2 NDC:82691-142-01 5 mL in 1 JAR; Type 0: Not a Combination Product 12/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/01/2017 Labeler - RV Skincare LLC (080986653)
