CLINIQUE BROAD SPECTRUM SPF 50 SUNSCREEN FACE WITH SOLAR SMART- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone cream 
CLINIQUE LABORATORIES LLC

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CLINIQUE BROAD SPECTRUM SPF 50 SUNSCREEN FACE CREAM WITH SOLAR SMART

Drug Facts

Active ingredients

Avobenzone 3.0%
Homosalate 5.0%
Octisalate 5.0%
Octocrylene 2.7%
Oxybenzone 5.0%

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 • methyl trimethicone • butylene glycol • butyloctyl salicylate • neopentyl glycol diheptanoate • butyrospermum parkii (shea butter) • peg-100 stearate • silica • dipentaerythrityl tri-polyhydroxystearate • lauryl peg-9 polydimethylsiloxyethyl dimethicone • dimethicone • glyceryl stearate • laurdimonium hydroxypropyl hydrolyzed soy protein • rosmarinus officinalis (rosemary) extract • perilla ocymoides leaf extract • plankton extract • caffeine • potassium cetyl phosphate • sucrose • styrene/acrylates copolymer • c30-38 olefin/isopropyl maleate/ma copolymer • cetyl alcohol • vp/eicosene copolymer • ethylhexylglycerin • ammonium acryloyldimethyltaurate/vp copolymer • peg-8 laurate • sodium rna • lecithin • propyl gallate • arginine ferulate • tocopheryl acetate • caprylyl glycol • ascorbyl tocopheryl maleate • stearic acid • xanthan gum • hexylene glycol • nordihydroguaiaretic acid • disodium edta • phenoxyethanol • mica • sodium dehydroacetate [iln37123]

Other information

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

PRINCIPAL DISPLAY PANEL - 50 ml Tube Carton

CLINIQUE

broad
spectrum
SPF 50
sunscreen
with
SolarSmart

UVA UVB
PROTECTION

face cream

1.7 FL. OZ.
50 ml e

PRINCIPAL DISPLAY PANEL - 50 ml Tube Carton
CLINIQUE BROAD SPECTRUM SPF 50 SUNSCREEN FACE WITH SOLAR SMART 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-065
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE50 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE27 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CETYL ALCOHOL (UNII: 936JST6JCN)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
PEG-8 LAURATE (UNII: 762O8IWA10)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
ARGININE FERULATE (UNII: 0774Y45BEE)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ASCORBYL TOCOPHERYL MALEATE (UNII: D2G6259XR5)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
XANTHAN GUM (UNII: TTV12P4NEE)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
MICA (UNII: V8A1AW0880)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
WATER (UNII: 059QF0KO0R)  
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
SHEA BUTTER (UNII: K49155WL9Y)  
PEG-100 STEARATE (UNII: YD01N1999R)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE (UNII: D21K655H52)  
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
ROSEMARY (UNII: IJ67X351P9)  
CAFFEINE (UNII: 3G6A5W338E)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-065-011 in 1 CARTON09/01/2010
150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02009/01/2010
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436manufacture(49527-065) , pack(49527-065) , label(49527-065)

Revised: 10/2023
Document Id: 079b3675-615e-1aac-e063-6394a90abb95
Set id: 8c7c0e3f-6092-413c-90f1-b3466c8a9501
Version: 7
Effective Time: 20231013
 
CLINIQUE LABORATORIES LLC