Label: CL EB MATTE MAKEUP BROAD SPECTRUM SPF 15- zinc oxide and titanium dioxide emulsion
- NDC Code(s): 49527-113-01, 49527-113-02
- Packager: CLINIQUE LABORATORIES LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 20, 2023
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- Active Ingredient
- Purpose
- Use
- Warnings
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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
dimethicone,water\aqua\eau,methyl trimethicone,peg-10 dimethicone,butylene glycol,butyloctyl salicylate,alcohol denat.,hamamelis virginiana (witch hazel) water,dimethicone/vinyl dimethicone crosspolymer,silica,hydrated silica,ascorbyl glucoside,magnesium ascorbyl phosphate,tetrahexyldecyl ascorbate,zinc pca,caffeine,sodium hyaluronate,laminaria saccharina extract,nylon-12,nylon-6,hydroxyapatite,silk powder\serica\poudre de soie,vinyl dimethicone/methicone silsesquioxane crosspolymer,trimethylsiloxysilicate/dimethiconol crosspolymer,dimethicone/peg-10/15 crosspolymer,polysilicone-11,lauryl peg-9 polydimethylsiloxyethyl dimethicone,propylene carbonate,alumina,disteardimonium hectorite,xanthan gum,dipropylene glycol,laureth-7,lecithin,sorbitan sesquioleate,triethoxycaprylylsilane,tocopherol,tocopheryl acetate,bht,sodium hydroxide,citric acid,tetrasodium edta,sodium citrate,phenoxyethanol,benzoic acid, [+/- titanium dioxide (ci 77891),iron oxides (ci 77491),iron oxides (ci 77492),iron oxides (ci 77499)] <iln50838>
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INGREDIENTS AND APPEARANCE
CL EB MATTE MAKEUP BROAD SPECTRUM SPF 15
zinc oxide and titanium dioxide emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49527-113 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 59 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 24 mg in 1 mL Inactive Ingredients Ingredient Name Strength ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW) POLICAPRAM (UNII: 14GUK8I73Z) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SACCHARINA LATISSIMA (UNII: 68CMP2MB55) BENZOIC ACID (UNII: 8SKN0B0MIM) VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) PROPYLENE CARBONATE (UNII: 8D08K3S51E) EDETATE SODIUM (UNII: MP1J8420LU) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) NYLON-12 (UNII: 446U8J075B) BOMBYX MORI FIBER (UNII: 6LK42KUV6W) XANTHAN GUM (UNII: TTV12P4NEE) SODIUM CITRATE (UNII: 1Q73Q2JULR) DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) ALUMINUM OXIDE (UNII: LMI26O6933) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) ALCOHOL (UNII: 3K9958V90M) PEG-10 DIMETHICONE (220 CST) (UNII: 287GF3Y3WC) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) HYDRATED SILICA (UNII: Y6O7T4G8P9) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) ZINC PIDOLATE (UNII: C32PQ86DH4) CAFFEINE (UNII: 3G6A5W338E) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) DIPROPYLENE GLYCOL (UNII: E107L85C40) LAURETH-7 (UNII: Z95S6G8201) SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) TOCOPHEROL (UNII: R0ZB2556P8) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SODIUM HYDROXIDE (UNII: 55X04QC32I) PHENOXYETHANOL (UNII: HIE492ZZ3T) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49527-113-01 1 in 1 CARTON 10/20/2023 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49527-113-02 1 in 1 CARTON 10/20/2023 2 5 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 10/20/2023 Labeler - CLINIQUE LABORATORIES LLC (044475127) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics Ltd 202952982 manufacture(49527-113) Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics Ltd. 204132062 pack(49527-113) , label(49527-113)
