CLINIQUE BROAD SPECTRUM SPF 30 OIL FREE FACE WITH SOLAR SMART- octinoxate, octisalate, titanium dioxide, and zinc oxide cream 
CLINIQUE LABORATORIES LLC

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CLINIQUE BROAD SPECTRUM SPF 30 OIL FREE FACE CREAM WITH SOLAR SMART

Drug Facts

Active ingredients

Octinoxate 7.5%
Octisalate 4.5%
Titanium dioxide 4.6%
Zinc oxide 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 • c12-15 alkyl benzoate • caprylyl methicone • neopentyl glycol diheptanoate • sucrose • polyglyceryl-10 pentastearate • pentylene glycol • ethylhexyl methoxycrylene • dimethicone • behenyl alcohol • peg-100 stearate • hydrogenated lecithin • butylene glycol • dipentaerythrityl tri-polyhydroxystearate • cucumis sativus (cucumber) fruit extract • hordeum vulgare (barley) extract\extrait d'orge • sigesbeckia orientalis (st. paul's wort) extract • glycerin • caffeine • sodium rna • sodium hyaluronate • tocopheryl acetate • propylene glycol dicaprate • isohexadecane • helianthus annuus (sunflower) seedcake • pvp/hexadecene copolymer • isostearic acid • sodium stearoyl lactylate • polyhydroxystearic acid • silica • acrylamide/sodium acryloyldimethyltaurate copolymer • xanthan gum • polysorbate 80 • dimethicone silylate • polyethylene • trisodium edta • bht • phenoxyethanol [iln43113]

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 30
sunscreen
with
SolarSmart+
UVA UVB
advanced
protection

oil-free
face cream

1.7 FL. OZ.
50 ml e

PRINCIPAL DISPLAY PANEL - 50 ml Tube Carton
CLINIQUE BROAD SPECTRUM SPF 30 OIL FREE FACE WITH SOLAR SMART 
octinoxate, octisalate, titanium dioxide, and zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-067
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE45 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE46 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
SUCROSE (UNII: C151H8M554)  
POLYGLYCERYL-10 PENTASTEARATE (UNII: PMX5872701)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DOCOSANOL (UNII: 9G1OE216XY)  
PEG-100 STEARATE (UNII: YD01N1999R)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE (UNII: D21K655H52)  
CUCUMBER (UNII: YY7C30VXJT)  
BARLEY (UNII: 5PWM7YLI7R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CAFFEINE (UNII: 3G6A5W338E)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
PROPYLENE GLYCOL DICAPRATE (UNII: U783H9JHWY)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
HELIANTHUS ANNUUS SEEDCAKE (UNII: 482WYF7XLC)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-067-011 in 1 CARTON01/01/2017
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 DrugM02001/01/2017
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder N.V.370151326manufacture(49527-067) , pack(49527-067) , label(49527-067)

Revised: 10/2023
Document Id: 079b699b-fbb1-0136-e063-6294a90a1447
Set id: 3d23406b-5252-4ab0-b666-77c0132b0d00
Version: 9
Effective Time: 20231013
 
CLINIQUE LABORATORIES LLC