Label: PERFECTIONIST PRO MULTI-DEFENSE UV FLUID BROAD SPRECTRUM SPF 45- titanium dioxide and zinc oxide lotion
- NDC Code(s): 11559-050-01
- Packager: ESTEE LAUDER INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 26, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
-
Uses
- helps prevent sunburn
- if used as directed with other sun protection measures (see Directions) decreases the risk of skin cancer and early skin aging caused by the sun
- Warnings
-
Directions
For sunscreen use:
- apply liberally and evenly 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 • dimethicone • butyloctyl salicylate • c12-15 alkyl benzoate • methyl trimethicone • isononyl isononanoate • diethylhexyl succinate • neopentyl glycol diheptanoate • butylene glycol • dipentaerythrityl tri-polyhydroxystearate • lauryl peg-9 polydimethylsiloxyethyl dimethicone • silica • trimethylsiloxysilicate • cetyl peg/ppg-10/1 dimethicone • hydroxyapatite • polygonum cuspidatum root extract • hordeum vulgare (barley) extract\extrait d'orge • triticum vulgare (wheat) germ extract • thermus thermophillus ferment • sodium hyaluronate • opuntia tuna extract • lilium tigrinum extract • algae extract • camellia sinensis (green tea) leaf extract • anthemis nobilis (chamomile) flower extract • caffeine • tocopheryl acetate • ergothioneine • squalane • glycerin • dimethicone silylate • hydrolyzed wheat protein/pvp crosspolymer • dimethicone crosspolymer-3 • glyceryl behenate/eicosadioate • stearalkonium hectorite • caprylyl glycol • isostearic acid • polyhydroxystearic acid • tetrahexyldecyl ascorbate • dipropylene glycol • triethoxycaprylylsilane • ethylbisiminomethylguaiacol manganese chloride • cyclodextrin • dimethicone/peg-10/15 crosspolymer • isopropyl myristate • propylene carbonate • bht • phenoxyethanol • red 28 lake (ci 45410) • blue 1 lake (ci 42090) <iln45003>
- Other information
- PRINCIPAL DISPLAY PANEL - 30 ml Container Carton
-
INGREDIENTS AND APPEARANCE
PERFECTIONIST PRO MULTI-DEFENSE UV FLUID BROAD SPRECTRUM SPF 45
titanium dioxide and zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11559-050 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 63 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) DIETHYLHEXYL SUCCINATE (UNII: 69W9UMG3P8) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE (UNII: D21K655H52) LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28) BARLEY (UNII: 5PWM7YLI7R) WHEAT (UNII: 4J2I0SN84Y) THERMUS THERMOPHILUS LYSATE (UNII: 775R692494) HYALURONATE SODIUM (UNII: YSE9PPT4TH) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CHAMOMILE (UNII: FGL3685T2X) CAFFEINE (UNII: 3G6A5W338E) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) ERGOTHIONEINE (UNII: BDZ3DQM98W) SQUALANE (UNII: GW89575KF9) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL BEHENATE/EICOSADIOATE (UNII: 73CJJ317SR) STEARALKONIUM HECTORITE (UNII: OLX698AH5P) CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISOSTEARIC ACID (UNII: X33R8U0062) TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ) DIPROPYLENE GLYCOL (UNII: E107L85C40) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ETHYLBISIMINOMETHYLGUAIACOL MANGANESE CHLORIDE (UNII: SM5YJ88LTU) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) PROPYLENE CARBONATE (UNII: 8D08K3S51E) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) PHENOXYETHANOL (UNII: HIE492ZZ3T) D&C RED NO. 28 (UNII: 767IP0Y5NH) ALUMINUM OXIDE (UNII: LMI26O6933) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11559-050-01 1 in 1 CARTON 10/05/2018 1 30 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 Drug M020 10/05/2018 Labeler - ESTEE LAUDER INC (005914387) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations Estee Lauder N.V. 370151326 manufacture(11559-050) , pack(11559-050) , label(11559-050)
