MOISTURE SURGE CC BROAD SPECTRUM SPF 30 HYDRATING COLOUR CORRECTOR- octinoxate, octisalate, titanium dioxide, and zinc oxide cream 
CLINIQUE LABORATORIES LLC

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MOISTURE SURGE CC

BROAD SPECTRUM SPF 30 HYDRATING COLOUR CORRECTOR

Drug Facts

Active ingredients

Octinoxate 7.5%
Octisalate 5.0%
Titanium dioxide 5.2%
Zinc oxide 3.2%

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 • squalane • octyldodecyl neopentanoate • butylene glycol • propanediol • glyceryl stearate • behenyl alcohol • peg-40 stearate • polyglyceryl-10 pentastearate • aloe barbadensis leaf water • thermus thermophillus ferment • trehalose • caffeine • glycerin • linoleic acid • lecithin • stearic acid • hydrogenated lecithin • sorbitol • polyglyceryl-6 polyricinoleate • tocopheryl acetate • ammonium acryloyldimethyltaurate/vp copolymer • sodium stearoyl lactylate • sodium hyaluronate • tetrahexyldecyl ascorbate • pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate • isopropyl titanium triisostearate • synthetic fluorphlogopite • xanthan gum • silica • alumina • sodium dehydroacetate • tin oxide • disodium edta • phenoxyethanol • [+/- mica • titanium dioxide (ci 77891) • iron oxides (ci 77492) • iron oxides (ci 77491) • iron oxides (ci 7799)] [iln39833]

Other information

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

CLINIQUE LABS., DIST.
NEW YORK, N.Y. 10022

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton

C

CLINIQUE

moisture surge
CC
cream
hydrating
colour corrector
broad spectrum
SPF 30

ALL SKIN TYPES

1.4 FL.OZ.LIQ./40 ml e

Principal Display Panel - 40 ml Bottle Carton
MOISTURE SURGE CC  BROAD SPECTRUM SPF 30 HYDRATING COLOUR CORRECTOR
octinoxate, octisalate, titanium dioxide, and zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-029
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) OCTISALATE50 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE52 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE32 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)  
POLYGLYCERYL-10 PENTASTEARATE (UNII: PMX5872701)  
WATER (UNII: 059QF0KO0R)  
SQUALANE (UNII: GW89575KF9)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PROPANEDIOL (UNII: 5965N8W85T)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
DOCOSANOL (UNII: 9G1OE216XY)  
PEG-40 STEARATE (UNII: ECU18C66Q7)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
TREHALOSE (UNII: B8WCK70T7I)  
CAFFEINE (UNII: 3G6A5W338E)  
GLYCERIN (UNII: PDC6A3C0OX)  
LINOLEIC ACID (UNII: 9KJL21T0QJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SORBITOL (UNII: 506T60A25R)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
STANNIC OXIDE (UNII: KM7N50LOS6)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
MICA (UNII: V8A1AW0880)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)  
MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-029-011 in 1 CARTON10/05/2022
140 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49527-029-0215 mL in 1 TUBE; Type 0: Not a Combination Product10/05/202212/31/2023
3NDC:49527-029-037 mL in 1 TUBE; Type 0: Not a Combination Product10/05/202212/31/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/05/2022
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder Cosmetics Ltd202952982manufacture(49527-029)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder Cosmetics Ltd.204132062pack(49527-029) , label(49527-029) , manufacture(49527-029)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436manufacture(49527-029) , label(49527-029) , pack(49527-029)
Establishment
NameAddressID/FEIBusiness Operations
PADC949264774label(49527-029) , pack(49527-029)

Revised: 1/2024
Document Id: 0e8855e7-139e-59ca-e063-6294a90a9f4e
Set id: ea4d564f-ac64-abac-e053-2a95a90a8abb
Version: 4
Effective Time: 20240109
 
CLINIQUE LABORATORIES LLC