Label: CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY PLUS FACE PROTECTOR BROAD SPECTRUM SPF 50- octinoxate, titanium dioxide, and zinc oxide lotion
- NDC Code(s): 49527-078-01
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 21, 2023
If you are a consumer or patient please visit this version.
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- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Use
- Warnings
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Directions
For sunscreen use:
- apply liberally 15 minutes before sun exposure
- reapply at least every two hours
- use a water resistant sunscreen if swimming or sweating
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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
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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:
- children under 6 months of age: ask a doctor
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Inactive ingredients
water\aqua\eau•dimethicone•butyloctyl salicylate•isononyl isononanoate•neopentyl glycol diheptanoate•lauryl peg-9 polydimethylsiloxyethyl dimethicone•butylene glycol•polydecene•polyhydroxystearic acid•ethylhexyl methoxycrylene•hydrated silica•dimethicone/vinyl dimethicone crosspolymer•trimethylsiloxysilicate•hydrolyzed wheat protein/pvp crosspolymer•hydroxyapatite•cetyl peg/ppg-10/1 dimethicone•dimethicone/peg-10/15 crosspolymer•sodium rna•quaternium-90 bentonite•sodium hyaluronate•dimethicone crosspolymer-3•styrene/acrylates copolymer•sodium chloride•caprylyl glycol•peg-8 laurate•propylene carbonate•silica•tocopherol•sodium citrate•disodium edta•bht•phenoxyethanol•potassium sorbate•iron oxides (ci 77491)•iron oxides (ci 77492) [iln47235]
- Other information
- PRINCIPAL DISPLAY PANEL - 40 ml Tube Carton
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INGREDIENTS AND APPEARANCE
CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY PLUS FACE PROTECTOR BROAD SPECTRUM SPF 50
octinoxate, titanium dioxide, and zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-078 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 50 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 32 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 36 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE 100 (UNII: RO266O364U) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA) 1,2-BUTANEDIOL (UNII: RUN0H01QEU) HYDROGENATED DIDECENE (UNII: 048B98MT5O) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8) HYDRATED SILICA (UNII: Y6O7T4G8P9) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW) (UNII: J2S07SB0YL) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) BIS-PEG-10 DIMETHICONE/DIMER DILINOLEATE COPOLYMER (UNII: CF5W1YCX11) SODIUM CARBONATE (UNII: 45P3261C7T) BENTONITE (UNII: A3N5ZCN45C) HYALURONATE SODIUM (UNII: YSE9PPT4TH) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR) SODIUM CHLORIDE (UNII: 451W47IQ8X) CAPRYLYL GLYCOL (UNII: 00YIU5438U) PEG-8 LAURATE (UNII: 762O8IWA10) PROPYLENE CARBONATE (UNII: 8D08K3S51E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TOCOPHEROL (UNII: R0ZB2556P8) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49527-078-01 1 in 1 CARTON 06/25/2020 1 40 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 06/25/2020 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations The Estee Lauder Inc 802599436 manufacture(49527-078) , pack(49527-078) , label(49527-078) Establishment Name Address ID/FEI Business Operations NORTHTEC KEYSTONE 949264774 pack(49527-078) , label(49527-078) Establishment Name Address ID/FEI Business Operations PALC 078364654 label(49527-078) , pack(49527-078)
