Label: DOLCE AND GABBANA MEET YOUR FLAWLESS MATTE SKIN DUO- octisalate, octocrylene, titanium dioxide, zinc oxide kit
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NDC Code(s):
23648-110-01,
23648-111-01,
23648-112-01,
23648-113-01, view more23648-114-01, 23648-115-01
- Packager: Socoplan
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 18, 2024
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
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Directions
- Apply generously 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 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
SHAKE WELL BEFORE USE
- Other information
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Inactive ingredients
WATER/EAU (AQUA), DIMETHICONE, CAPRYLYL METHICONE, TRIMETHYLSILOXYSILICATE, METHYL TRIMETHICONE, POLYMETHYLSILSESQUIOXANE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, BUTYLENE GLYCOL, PEG-10 DIMETHICONE, PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER, CAPRYLYL DIMETHICONE ETHOXY GLUCOSIDE, POLYIMIDE-1, CETEARYL DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, POLYPHENYLSILSESQUIOXANE, PHENOXYETHANOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, GLYCERIN, SODIUM CHLORIDE, POTASSIUM SORBATE, SODIUM DEHYDROACETATE, ALUMINA, TRIETHOXYCAPRYLSILANE, C20-24 OLEFIN, SILICA, TOCOPHERYL ACETATE, PERSEA GRATISSIMA (AVOCADO) FRUIT EXTRACT, PUNICA GRANATUM PERICARP EXTRACT, LAURYL DIMETHICONE, OPUNTIA TUNA FRUOT EXTRACT, TOCOPHEROL; +/- MAY CONTAIN: TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499)
- Package Labeling:Kit
- Package Labeling:
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INGREDIENTS AND APPEARANCE
DOLCE AND GABBANA MEET YOUR FLAWLESS MATTE SKIN DUO
octisalate, octocrylene, titanium dioxide, zinc oxide kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:23648-110 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23648-110-01 1 in 1 KIT 05/01/2024 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BLISTER PACK 0.6 mL Part 2 1 BLISTER PACK 0.6 mL Part 3 1 BLISTER PACK 0.6 mL Part 4 1 BLISTER PACK 0.6 mL Part 5 1 BLISTER PACK 0.6 mL Part 1 of 5 DOLCE AND GABBANA EVERLAST FOUNDATION - 5N
octisalate, octocrylene, titanium dioxide, zinc oxide emulsionProduct Information Item Code (Source) NDC:23648-111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 35 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 5 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 18.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL METHICONE (UNII: Q95M2P1KJL) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO) CAPRYLYL DIMETHICONE ETHOXY GLUCOSIDE (UNII: DAC8GQQ57F) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) ALUMINA (UNII: LMI26O6933) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) AVOCADO (UNII: SDS87L369F) POMEGRANATE FRUIT RIND (UNII: RS999V57DU) OPUNTIA TUNA FRUIT (UNII: 75UY509K9B) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23648-111-01 1 in 1 CARTON 1 0.6 mL in 1 BLISTER PACK; 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 05/01/2024 Part 2 of 5 DOLCE AND GABBANA EVERLAST FOUNDATION - 5N
octisalate, octocrylene, titanium dioxide, zinc oxide emulsionProduct Information Item Code (Source) NDC:23648-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 35 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 5 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 18.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL METHICONE (UNII: Q95M2P1KJL) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO) CAPRYLYL DIMETHICONE ETHOXY GLUCOSIDE (UNII: DAC8GQQ57F) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) ALUMINA (UNII: LMI26O6933) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) AVOCADO (UNII: SDS87L369F) POMEGRANATE FRUIT RIND (UNII: RS999V57DU) OPUNTIA TUNA FRUIT (UNII: 75UY509K9B) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23648-112-01 1 in 1 CARTON 1 0.6 mL in 1 BLISTER PACK; 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 05/01/2024 Part 3 of 5 DOLCE AND GABBANA EVERLAST FOUNDATION - 5N
octisalate, octocrylene, titanium dioxide, zinc oxide emulsionProduct Information Item Code (Source) NDC:23648-113 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 35 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 5 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 18.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL METHICONE (UNII: Q95M2P1KJL) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO) CAPRYLYL DIMETHICONE ETHOXY GLUCOSIDE (UNII: DAC8GQQ57F) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) ALUMINA (UNII: LMI26O6933) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) AVOCADO (UNII: SDS87L369F) POMEGRANATE FRUIT RIND (UNII: RS999V57DU) OPUNTIA TUNA FRUIT (UNII: 75UY509K9B) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23648-113-01 1 in 1 CARTON 1 0.6 mL in 1 BLISTER PACK; 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 05/01/2024 Part 4 of 5 DOLCE AND GABBANA EVERLAST FOUNDATION - 5N
octisalate, octocrylene, titanium dioxide, zinc oxide emulsionProduct Information Item Code (Source) NDC:23648-114 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 35 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 5 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 18.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL METHICONE (UNII: Q95M2P1KJL) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO) CAPRYLYL DIMETHICONE ETHOXY GLUCOSIDE (UNII: DAC8GQQ57F) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) ALUMINA (UNII: LMI26O6933) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) AVOCADO (UNII: SDS87L369F) POMEGRANATE FRUIT RIND (UNII: RS999V57DU) OPUNTIA TUNA FRUIT (UNII: 75UY509K9B) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23648-114-01 1 in 1 CARTON 1 0.6 mL in 1 BLISTER PACK; 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 05/01/2024 Part 5 of 5 DOLCE AND GABBANA EVERLAST FOUNDATION - 5N
octisalate, octocrylene, titanium dioxide, zinc oxide emulsionProduct Information Item Code (Source) NDC:23648-115 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 35 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 50 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 5 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 18.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) CAPRYLYL METHICONE (UNII: Q95M2P1KJL) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG-12 DIMETHICONE/PPG-20 CROSSPOLYMER (UNII: 965K72OQXO) CAPRYLYL DIMETHICONE ETHOXY GLUCOSIDE (UNII: DAC8GQQ57F) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U) GLYCERIN (UNII: PDC6A3C0OX) SODIUM CHLORIDE (UNII: 451W47IQ8X) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) ALUMINA (UNII: LMI26O6933) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) AVOCADO (UNII: SDS87L369F) POMEGRANATE FRUIT RIND (UNII: RS999V57DU) OPUNTIA TUNA FRUIT (UNII: 75UY509K9B) TOCOPHEROL (UNII: R0ZB2556P8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:23648-115-01 1 in 1 CARTON 1 0.6 mL in 1 BLISTER PACK; 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 05/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/01/2024 Labeler - Socoplan (276221405) Establishment Name Address ID/FEI Business Operations Socoplan 276221405 pack(23648-110)