CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY PLUS FACE PROTECTOR BROAD SPECTRUM SPF 50- octinoxate, titanium dioxide, and zinc oxide lotion 
CLINIQUE LABORATORIES LLC

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CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY + FACE PROTECTOR BROAD SPECTRUM SPF 50

Drug Facts

Active ingredients

Octinoxate 5.0%
Titanium Dioxide 3.2%
Zinc Oxide 3.6%

Purpose

Sunscreen

Use

helps prevent sunburn

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

For sunscreen use:

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

protect the product in this container from excessive heat and direct sun

PRINCIPAL DISPLAY PANEL - 40 ml Tube Carton

sun protection

SUPERDEFENSE
CITY BLOCK

daily energy + face protector

BROAD
SPECTRUM
SPF 50

CLINIQUE

1.4 FL.OZ.LIQ./
40 ml e

PRINCIPAL DISPLAY PANEL - 40 ml Tube Carton
CLINIQUE SUPER DEFENSE CITY BLOCK DAILY ENERGY PLUS FACE PROTECTOR BROAD SPECTRUM SPF 50 
octinoxate, titanium dioxide, and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-078
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE32 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE36 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-078-011 in 1 CARTON06/25/2020
140 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/25/2020
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436manufacture(49527-078) , pack(49527-078) , label(49527-078)
Establishment
NameAddressID/FEIBusiness Operations
NORTHTEC KEYSTONE949264774pack(49527-078) , label(49527-078)
Establishment
NameAddressID/FEIBusiness Operations
PALC078364654label(49527-078) , pack(49527-078)

Revised: 12/2023
Document Id: 0d0e08b5-1d53-f62b-e063-6294a90ace87
Set id: d1a3d76f-16dd-4533-8144-9a3175f6e15f
Version: 11
Effective Time: 20231221
 
CLINIQUE LABORATORIES LLC