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

REDNESS solutions DAILY PROTECTIVE BASE BROAD SPECTRUM SPF 15 by

Drug Labeling and Warnings

REDNESS solutions DAILY PROTECTIVE BASE BROAD SPECTRUM SPF 15 by is a Otc medication manufactured, distributed, or labeled by CLINIQUE LABORATORIES LLC, Estee Lauder Companies Inc., PALC, Estee Lauder Cosmetics Ltd., Whitman Laboratories Ltd., Estee Lauder N.V., The Estee Lauder Inc, Northtec LLC, PADC 1. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

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:

• apply liberally 15 minutes before sun exposure
• reapply at least every two hours
• use a water resistant sunscreen if swimming or sweating
• Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
  • limit time in the sun, especially from 10 a.m. – 2 p.m.
  • wear long-sleeved shirts, pants, hats and sunglasses
• children under 6 months of age: ask a doctor

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

INGREDIENTS AND APPEARANCE

REDNESS SOLUTIONS DAILY PROTECTIVE BASE BROAD SPECTRUM SPF 15 
titanium dioxide and zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49527-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	0.0698 g  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	0.0268 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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)
lactobacillus 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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49527-019-01	1 in 1 CARTON	12/01/2011
1		40 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	12/01/2011

Labeler - CLINIQUE LABORATORIES INC. (173047747)

Establishment
Name	Address	ID/FEI	Business Operations
ESTEE LAUDER COMPANY, THE		828534516	RELABEL(49527-019) , REPACK(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
ESTEE LAUDER COSMETICS, LTD		244669714	MANUFACTURE(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
ESTEE LAUDER COSMETICS, LTD.		202952982	MANUFACTURE(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
ESTEE LAUDER N.V.		370151326	MANUFACTURE(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
LEN-RON MANUFACTURING DIVISION OF ARAMIS INC		809771152	MANUFACTURE(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
NORTHTEC INC		943871157	RELABEL(49527-019) , REPACK(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
PADC 1		949264774	RELABEL(49527-019) , REPACK(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
WHITMAN LABORATORIES, LTD.		216866277	MANUFACTURE(49527-019)

Establishment
Name	Address	ID/FEI	Business Operations
ESTEE LAUDER COSMETICS, LTD		255175580	MANUFACTURE(49527-019)