Label: BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40- octinoxate, titanium dioxide, and zinc oxide liquid
- NDC Code(s): 64141-031-01
- Packager: Bobbi Brown Professional Cosmetics Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
- Use
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Warnings
For external use only
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 and evenly 15 minutes before sun exposure
- reapply at least every two hours
- use a water resistant sunscreen if swimming or sweating
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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 • octyldodecyl neopentanoate • butyloctyl salicylate • methyl trimethicone • isononyl isononanoate • butylene glycol • diethylhexyl succinate • lauryl peg-9 polydimethylsiloxyethyl dimethicone • cetyl peg/ppg-10/1 dimethicone • laureth-4 • tocopheryl acetate • sodium hyaluronate • citrullus lanatus (watermelon) fruit extract • litchi chinensis seed extract • sapindus mukorossi fruit extract • laminaria saccharina extract • lens esculenta (lentil) fruit extract • polygonum cuspidatum root extract • hippophae rhamnoides extract • ganoderma lucidum (mushroom) extract • pyrus malus (apple) fruit extract • panax ginseng (ginseng) root extract • cordyceps sinensis extract • lavandula angustifolia (lavender) oil • sasa kurilensis water • glycerin • methicone • sodium pca • sodium lactate • hydrolyzed wheat protein/ pvp crosspolymer • dimethicone crosspolymer-3 • dimethicone/vinyl dimethicone crosspolymer • thermus thermophillus ferment • caesalpinia spinosa gum • magnesium sulfate • aluminum hydroxide • dextrin • dimethicone/peg-10/15 crosspolymer • caprylyl glycol • dipropylene glycol • dipentaerythrityl tri-polyhydroxystearate • stearic acid • linalool • bht • disodium edta • sodium citrate • phenoxyethanol • potassium sorbate • sodium benzoate • [+/- mica • titanium dioxide (ci 77891) • iron oxides (ci 77491) • iron oxides (ci 77492) • iron oxides (ci 77499)] <iln48151>
- PRINCIPAL DISPLAY PANEL - 30 ml Tube Carton
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INGREDIENTS AND APPEARANCE
BOBBI BROWN INTENSIVE SERUM FOUNDATION BROAD SPECTRUM SPF 40
octinoxate, titanium dioxide, and zinc oxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64141-031 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 40 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 62 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 39 mg in 1 mL Inactive Ingredients Ingredient Name Strength SASA KURILENSIS WHOLE (UNII: X399JB9XAS) GLYCERIN (UNII: PDC6A3C0OX) METHICONE (20 CST) (UNII: 6777U11MKT) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) SODIUM LACTATE (UNII: TU7HW0W0QT) HYDROLYZED WHEAT PROTEIN (ENZYMATIC; 3000 MW) (UNII: J2S07SB0YL) DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ) THERMUS THERMOPHILUS (UNII: 415H64SACF) CAESALPINIA SPINOSA WHOLE (UNII: O759MFY23D) MAGNESIUM SULFATE ANHYDROUS (UNII: ML30MJ2U7I) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3) DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS) CAPRYLYL GLYCOL (UNII: 00YIU5438U) DIPROPYLENE GLYCOL (UNII: E107L85C40) DIPENTAERYTHRITYL TRI-POLYHYDROXYSTEARATE (UNII: D21K655H52) STEARIC ACID (UNII: 4ELV7Z65AP) LINALOOL OXIDE (UNII: 4UJJ55KMCS) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) DISODIUM EDTA-COPPER (UNII: 6V475AX06U) SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR) PHENOXYETHANOL (UNII: HIE492ZZ3T) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) SODIUM BENZOATE (UNII: OJ245FE5EU) MICA (UNII: V8A1AW0880) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) ISONONYL ISONONANOATE (UNII: S4V5BS6GCX) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) DIETHYLHEXYL SUCCINATE (UNII: 69W9UMG3P8) LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2) (UNII: V2W71V8T0X) LAURETH-4 (UNII: 6HQ855798J) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) HYALURONATE SODIUM (UNII: YSE9PPT4TH) WATERMELON (UNII: 231473QB6R) LITCHI CHINENSIS SEED (UNII: 9294024N9Q) SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y) SACCHARINA LATISSIMA (UNII: 68CMP2MB55) LENS CULINARIS FRUIT (UNII: ZYZ076G9JH) REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7) HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T) REISHI (UNII: TKD8LH0X2Z) APPLE (UNII: B423VGH5S9) PANAX GINSENG ROOT OIL (UNII: P9T4K47OM0) OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU) LAVENDER OIL (UNII: ZBP1YXW0H8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64141-031-01 1 in 1 CARTON 01/27/2021 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 01/27/2021 Labeler - Bobbi Brown Professional Cosmetics Inc. (627131279) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics Ltd. 202952982 manufacture(64141-031) Establishment Name Address ID/FEI Business Operations Estee Lauder Cosmetics Ltd. 204132062 pack(64141-031) , label(64141-031)
