REVLON COLORSTAY LIQUID MAKEUP FOR NORMAL TO DRY SKIN- zinc oxide, titanium dioxide make-up liquid

Revlon Colorstay Liquid Makeup for Normal to Dry Skin by

Drug Labeling and Warnings

Revlon Colorstay Liquid Makeup for Normal to Dry Skin by is a Otc medication manufactured, distributed, or labeled by Revlon Consumer Products Corp, REVLON, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients:

Titanium Dioxide 4.3%

Zinc Oxide 2.1%

Warnings:

For external use only. Avoid contact with eyes. Discount use if signs of irritation or rash appear. Apply prior to sun exposure

Inactive Ingredients:

CYCLOPENTASILOXANE,AQUA ((WATER) EAU),DIMETHICONE,TRIMETHYLSILOXYSILICATE,PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE,PHENYL TRIMETHICONE,BUTYLENE GLYCOL,SILICA,METHYL METHACRYLATE CROSSPOLYMER,NYLON-12,DIMETHICONE/PEG-10/15 CROSSPOLYMER,TRIBEHENIN,ALUMINA,MAGNESIUM SULFATE,LAURETH-7,POLYGLYCERYL-3 DIISOSTEARATE,PHENOXYETHANOL,METHICONE,ETHYLPARABEN,METHYLPARABEN,DISTEARDIMONIUM HECTORITE,ETHYLENE BRASSYLATE,TRIETHOXYCAPRYLYLSILANE,TOCOPHERYL ACETATE,TRIETHYL CITRATE,TETRASODIUM EDTA,TOCOPHEROL,SODIUM CITRATE,DIPROPYLENE GLYCOL ,BISABOLOL,ETHYLHEXYL PALMITATE,PEG-12 GLYCERYL DIMYRISTATE,SALICYLIC ACID ,CYCLOHEXASILOXANE,DIMETHICONE/SILSESQUIOXANE COPOLYMER,SILICA DIMETHYL SILYATE,POLYSORBATE 20,AMMONIUM POLYACRYLOYLDIMETHYL TAURATE,CAPRYLYL GLYCOL,SERICA ((SILK) SOIE),CYMBIDIUM GRANDIFLORUM (ORCHID) FLOWER EXTRACT ,LACTOBACILLUS/ERIODICTYON CALIFORNICUM FERMENT EXTRACT,LILIUM CANDIDUM (LILY) BULB EXTRACT,MALVA SYLVESTRIS (MALLOW) EXTRACT,SODIUM HYALURONATE

May Contain Mica, Titanium Dioxide (Ci 77891), Iron Oxides (CI 77491, 77492, 77499), Zinc Oxide (CI 77647)

Purpose

Sunscreen

To Use

Shake well. Apply to one area at a time, blending quickly. Remove with facial cleanser.

Principal Display Panel:

​REVLON

Colorstay Makeup

Normal/Dry Skin

SPF 20

INGREDIENTS AND APPEARANCE

REVLON COLORSTAY LIQUID MAKEUP FOR NORMAL TO DRY SKIN 
zinc oxide, titanium dioxide make-up liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10967-643
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	2.1 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
METHICONE (20 CST) (UNII: 6777U11MKT)
LAURETH-7 (UNII: Z95S6G8201)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPARABEN (UNII: A2I8C7HI9T)
ETHYLPARABEN (UNII: 14255EXE39)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: TYP81E471F)
TRIBEHENIN (UNII: 8OC9U7TQZ0)
NYLON-12 (UNII: 446U8J075B)
ALUMINUM OXIDE (UNII: LMI26O6933)
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE SODIUM (UNII: MP1J8420LU)
LEVOMENOL (UNII: 24WE03BX2T)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
TOCOPHEROL (UNII: R0ZB2556P8)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
SALICYLIC ACID (UNII: O414PZ4LPZ)
MALVA SYLVESTRIS FLOWERING TOP (UNII: X1U1U0N90J)
LILIUM CANDIDUM BULB (UNII: AHG15J8AM0)
CYMBIDIUM HOOKERIANUM FLOWER (UNII: H2DJ03DI5I)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PEG-12 GLYCERYL DIMYRISTATE (UNII: VS4W16AQ3X)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10967-643-01	30 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product	06/01/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	06/01/2012

Labeler - Revlon Consumer Products Corp (788820165)

Establishment
Name	Address	ID/FEI	Business Operations
REVLON, INC.		809725570	manufacture(10967-643)