PEP-STAR DAILY UV PROTECTOR BROAD SPECTRUM SPF 50- titanium dioxide and zinc oxide lotion 
CLINIQUE LABORATORIES LLC

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PEP-START DAILY UV PROTECTOR BROAD SPECTRUM SPF 50

Drug Facts

Active ingredients

Titanium Dioxide 6.3%
Zinc Oxide 4.0%

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 • dimethicone • butyloctyl salicylate • polydiethylsiloxane • c12-15 alkyl benzoate • isononyl isononanoate • diethylhexyl succinate • neopentyl glycol diheptanoate • methyl trimethicone • butylene glycol • ethylhexyl methoxycrylene • lauryl peg-9 polydimethylsiloxyethyl ethylhexyl dimethicone • silica • laureth-4 • cetyl peg/ppg-10/1 dimethicone • dipentaerythrityl tri-polyhydroxystearate • hydrolyzed wheat protein/pvp crosspolymer • caprylyl glycol • dimethicone silylate • dimethicone/peg-10/15 crosspolymer • isostearic acid • dimethicone crosspolymer-3 • polyhydroxystearic acid • triethoxycaprylylsilane • dipropylene glycol • phenoxyethanol • iron oxides (ci 77491) • iron oxides (ci 77492) [iln43311]

Other information

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

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Carton

CLINIQUE

pep-start

daily UV protector
broad spectrum
SPF 50

1 FL.OZ.LIQ./30 ml e

PRINCIPAL DISPLAY PANEL - 30 ml Bottle Carton
PEP-STAR DAILY UV PROTECTOR BROAD SPECTRUM SPF 50 
titanium dioxide and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-073
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE63 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE40 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
DIETHYLHEXYL SUCCINATE (UNII: 69W9UMG3P8)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
LAURETH-4 (UNII: 6HQ855798J)  
DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE (UNII: D21K655H52)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-073-011 in 1 CARTON01/01/2017
130 mL in 1 BOTTLE; 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
The Estee Lauder Inc802599436manufacture(49527-073) , pack(49527-073) , label(49527-073)

Revised: 10/2023
Document Id: 079bb7e2-552c-cf0e-e063-6394a90a74c8
Set id: 68cfcbc2-a214-437e-9956-f77c90d74888
Version: 9
Effective Time: 20231013
 
CLINIQUE LABORATORIES LLC