MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25- octinoxate, octisalate, titanium dioxide, and zinc oxide cream 
CLINIQUE LABORATORIES LLC

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MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25

Drug Facts

Active ingredients

Octinoxate 7.5%
Octisalate 4.5%
Titanium dioxide 3.8%
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 • c12-15 alkyl benzoate • caprylyl methicone • neopentyl glycol diheptanoate • butylene glycol • pentylene glycol • glycerin • polyglyceryl-10 pentastearate • hydrogenated lecithin • behenyl alcohol • peg-100 stearate • sucrose • laminaria saccharina extract • cucumis sativus (cucumber) fruit extract • aloe barbadensis leaf water • hordeum vulgare (barley) extract\extrait d'orge • caffeine • tocopheryl acetate • isohexadecane • lecithin • sodium stearoyl lactylate • propylene glycol dicaprate • sodium hyaluronate • helianthus annuus (sunflower) seedcake • trehalose • isostearic acid • polyhydroxystearic acid • polysorbate 80 • dimethicone • xanthan gum • polyethylene • acrylamide/sodium acryloyldimethyltaurate copolymer • silica • disodium edta • tetrasodium edta • bht • phenoxyethanol • [+/- titanium dioxide (ci 77891) • iron oxides (ci 77491) • iron oxides (ci 77492) • iron oxides (ci 77499)] [iln45300]

Other information

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

PRINCIPAL DISPLAY PANEL - 40 ml Tube Carton

hydration

CLINIQUE

moisture surge

sheertint hydrator
broad spectrum
SPF 25

MIMETIC-SHADE™ TECHNOLOGY

1.4 FL.OZ.LIQ./40 ml e

PRINCIPAL DISPLAY PANEL - 40 ml Tube Carton
MOISTURE SURGE SHEERTINT HYDRATOR BROAD SPECTRUM SPF 25 
octinoxate, octisalate, titanium dioxide, and zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-074
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 DIOXIDE38 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE36 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYGLYCERYL-10 PENTASTEARATE (UNII: PMX5872701)  
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)  
DOCOSANOL (UNII: 9G1OE216XY)  
PEG-100 STEARATE (UNII: YD01N1999R)  
SUCROSE (UNII: C151H8M554)  
SACCHARINA LATISSIMA (UNII: 68CMP2MB55)  
CUCUMBER (UNII: YY7C30VXJT)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
BARLEY (UNII: 5PWM7YLI7R)  
CAFFEINE (UNII: 3G6A5W338E)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)  
PROPYLENE GLYCOL DICAPRATE (UNII: U783H9JHWY)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
HELIANTHUS ANNUUS SEEDCAKE (UNII: 482WYF7XLC)  
TREHALOSE (UNII: B8WCK70T7I)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
XANTHAN GUM (UNII: TTV12P4NEE)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
EDETATE SODIUM (UNII: MP1J8420LU)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
WATER (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-074-011 in 1 CARTON10/16/2019
140 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:49527-074-021 mL in 1 TUBE; Type 0: Not a Combination Product10/16/201910/13/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/16/2019
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder Cosmetics Ltd.202952982manufacture(49527-074)
Establishment
NameAddressID/FEIBusiness Operations
Estee Lauder Cosmetics Ltd.204132062label(49527-074) , pack(49527-074)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436manufacture(49527-074) , pack(49527-074) , label(49527-074)

Revised: 10/2023
Document Id: 079c68e7-7fd2-9bb9-e063-6394a90a5f8e
Set id: 159410d4-4479-4442-b371-bde72aae3e1e
Version: 7
Effective Time: 20231013
 
CLINIQUE LABORATORIES LLC