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

  • NDC Code(s): 10967-643-01
  • Packager: Revlon Consumer Products Corp
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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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Updated October 21, 2021

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  • Active Ingredients:

    Titanium Dioxide 4.3 %

    Zinc Oxide (nano) 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, Methyl Methacrylate Crosspolymer, Silica, Butylene Glycol, Nylon-12, Dimethicone/PEG-10/15 Crosspolymer, Alumina, Disteardimonium Hectorite, Ethylene Brassylate, Hydrogen Dimethicone, Hydrolyzed Vegetable Protein, Laureth-7, Magnesium Sulfate, Methicone, Mica, Polyglyceryl-3 Diisostearate, Salicylic Acid, Sodium Hyaluronate, Tetrasodium EDTA, Tocopheryl Acetate, Tribehenin, Triethoxycaprylylsilane, Triethyl Citrate, Ethylparaben, Methylparaben, Phenoxyethanol.

    MAY CONTAIN:

    [Iron Oxides (CI 77491), Iron Oxides (CI 77492), Iron Oxides (CI 77499), Titanium Dioxide (CI 77891)] B02217

  • Purpose

    Sunscreen

  • To Use

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

  • Front and Back Label_Revlon Colorstay Normal to Dry Foundation

    Principle Display PanelFront and Back Label_ Colorstay Normal to Dry Foundation

    SPF 20

  • INGREDIENTS AND APPEARANCE
    REVLON COLORSTAY LIQUID MAKEUP FOR NORMAL TO DRY SKIN 
    zinc oxide, titanium dioxide make-up liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10967-643
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION2.1 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE4.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    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 CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10967-643-0130 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product06/01/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35206/01/2012
    Labeler - Revlon Consumer Products Corp (788820165)
    Establishment
    NameAddressID/FEIBusiness Operations
    REVLON, INC.809725570manufacture(10967-643)
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