REDNESS SOLUTIONS DAILY PROTECTIVE BASE BROAD SPECTRUM SPF 15- titanium dioxide and zinc oxide cream 
CLINIQUE LABORATORIES LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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REDNESS SOLUTIONS DAILY PROTECTIVE BASE BROAD SPECTRUM SPF 15

Drug Facts

Active ingredients

Titanium dioxide 6.5%

Zinc oxide 2.5%

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 • octyldodecyl neopentanoate • c12-15 alkyl benzoate • butylene glycol • tricaprylyl citrate • steareth-2 trioctyldodecyl citrate • glyceryl stearate • peg-100 stearate • barium sulfate • silica • ascophyllum nodosum extract • asparagopsis armata extract • sea whip extract • tocopheryl acetate • sucrose • pantethine • caffeine • dimethicone • cetearyl alcohol • isostearic acid • polyhydroxystearic acid • bisabolol • magnesium ascorbyl phosphate • lactobacillus ferment • sodium hyaluronate • sorbitol • phytosphingosine • caprylyl glycol • aluminum hydroxide • stearic acid • hexylene glycol • xanthan gum • disodium edta • phenoxyethanol • iron oxides (ci 77491, ci 77492, ci 77499) • chromium hydroxide green (ci 77289) [iln39531]

Other information

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

PRINCIPAL DISPLAY PANEL - 40 ml Bottle Carton

redness

CLINIQUE

redness
solutions

daily
protective base
broad spectrum
SPF 15

ALL SKIN TYPES

1.35 FL.OZ.LIQ./40 ml e

Principal Display Panel - 40 ml Bottle Carton
REDNESS SOLUTIONS DAILY PROTECTIVE BASE BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49527-019
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE65 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
METHYL TRIMETHICONE (UNII: S73ZQI0GXM)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
TRICAPRYLYL CITRATE (UNII: BXW1GAI4TA)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
BARIUM SULFATE (UNII: 25BB7EKE2E)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
PSEUDOPTEROGORGIA ELISABETHAE (UNII: UDY3H1OUX5)  
SUCROSE (UNII: C151H8M554)  
PANTETHINE (UNII: 7K81IL792L)  
CAFFEINE (UNII: 3G6A5W338E)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
LEVOMENOL (UNII: 24WE03BX2T)  
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
LIMOSILACTOBACILLUS REUTERI (UNII: 9913I24QEE)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SORBITOL (UNII: 506T60A25R)  
PHYTOSPHINGOSINE (UNII: GIN46U9Q2Q)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
CHROMIUM HYDROXIDE GREEN (UNII: RV8FT8XF5R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:49527-019-011 in 1 CARTON12/01/2011
140 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49527-019-0215 mL in 1 TUBE; Type 0: Not a Combination Product12/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM02012/01/2011
Labeler - CLINIQUE LABORATORIES LLC (044475127)
Registrant - Estee Lauder Companies Inc. (790802086)
Establishment
NameAddressID/FEIBusiness Operations
The Estee Lauder Inc802599436pack(49527-019) , label(49527-019) , manufacture(49527-019)
Establishment
NameAddressID/FEIBusiness Operations
NORTHTEC LLC943871157pack(49527-019) , label(49527-019)

Revised: 9/2023
Document Id: 04a34025-eae3-0729-e063-6394a90a9f31
Set id: d4133b2c-54e1-43de-98b4-7908a52f0905
Version: 9
Effective Time: 20230905
 
CLINIQUE LABORATORIES LLC