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

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CLINIQUE BROAD SPECTRUM SPF 50 SUNSCREEN BODY 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 • 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 • arginine ferulate • tocopheryl acetate • caprylyl glycol • propyl gallate • ascorbyl tocopheryl maleate • stearic acid • xanthan gum • hexylene glycol • nordihydroguaiaretic acid • disodium edta • phenoxyethanol • mica • sodium dehydroacetate [iln37121]

Other information

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

PRINCIPAL DISPLAY PANEL - 150 ml Tube Carton

CLINIQUE

broad
spectrum
SPF 50
sunscreen
with
SolarSmart

UVA UVB
PROTECTION

body cream

5 FL. OZ.
150 ml e

PRINCIPAL DISPLAY PANEL - 150 ml Tube Carton
CLINIQUE BROAD SPECTRUM SPF 50 SUNSCREEN BODY WITH SOLAR SMART 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-069
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
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)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
PEG-8 LAURATE (UNII: 762O8IWA10)  
ARGININE FERULATE (UNII: 0774Y45BEE)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
PROPYL GALLATE (UNII: 8D4SNN7V92)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-069-011 in 1 CARTON06/01/2011
1150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/01/2011
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436manufacture(49527-069) , pack(49527-069) , label(49527-069)

Revised: 10/2023
Document Id: 079bb65e-7a67-6c0a-e063-6294a90ab33a
Set id: 94274343-3892-4c27-9d2f-c025310e2959
Version: 9
Effective Time: 20231013
 
CLINIQUE LABORATORIES LLC