Label: BOBBI BROWN SPF 50 PROTECTIVE FACE BASE BROAD SPECTRUM- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
- NDC Code(s): 64141-014-01
- Packager: Bobbi Brown Professional Cosmetics Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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 Ingredients
- Purpose
- Use
- Warnings
-
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
water\aqua\eau • butyloctyl salicylate • methyl trimethicone • neopentyl glycol diheptanoate • aleurites moluccana (kukui) seed oil • lauryl peg-9 polydimethylsiloxyethyl dimethicone • peg-100 stearate • butylene glycol • glyceryl stearate • dipentaerythrityl tri-polyhydroxystearate • laminaria ochroleuca extract • laminaria digitata extract • algae extract • lavandula angustifolia (lavender) • pelargonium graveolens (geranium) flower oil • sodium hyaluronate • caffeine • ergothioneine • sorbitol • ethylhexylglycerin • potassium cetyl phosphate • cetyl alcohol • vp/eicosene copolymer • saccharide isomerate • caprylic/capric triglyceride • caprylyl glycol • ammonium acryloyldimethyltaurate/vp copolymer • stearic acid • dehydroxanthan gum • sodium dehydroacetate • disodium edta • phenoxyethanol • citric acid • citronellol • geraniol • linalool • mica <iln39524>
- Other information
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton
-
INGREDIENTS AND APPEARANCE
BOBBI BROWN SPF 50 PROTECTIVE FACE BASE BROAD SPECTRUM
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64141-014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 0.29124 g in 1 mL HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 0.04854 g in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 0.04854 g in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 0.0262116 g in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 0.029124 g in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) METHYL TRIMETHICONE (UNII: S73ZQI0GXM) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) KUKUI NUT OIL (UNII: TP11QR7B8R) PEG-100 STEARATE (UNII: YD01N1999R) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) LAMINARIA OCHROLEUCA (UNII: 4R2124HE76) LAMINARIA DIGITATA (UNII: 15E7C67EE8) LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P) PELARGONIUM GRAVEOLENS FLOWER OIL (UNII: 3K0J1S7QGC) HYALURONATE SODIUM (UNII: YSE9PPT4TH) CAFFEINE (UNII: 3G6A5W338E) ERGOTHIONEINE (UNII: BDZ3DQM98W) SORBITOL (UNII: 506T60A25R) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) CETYL ALCOHOL (UNII: 936JST6JCN) SACCHARIDE ISOMERATE (UNII: W8K377W98I) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CAPRYLYL GLYCOL (UNII: 00YIU5438U) AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) STEARIC ACID (UNII: 4ELV7Z65AP) SODIUM DEHYDROACETATE (UNII: 8W46YN971G) EDETATE DISODIUM (UNII: 7FLD91C86K) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) GERANIOL (UNII: L837108USY) LINALOOL, (+/-)- (UNII: D81QY6I88E) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64141-014-01 1 in 1 CARTON 09/01/2012 08/18/2023 1 50 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 09/01/2012 08/18/2023 Labeler - Bobbi Brown Professional Cosmetics Inc. (627131279) Registrant - Estee Lauder Companies Inc. (790802086) Establishment Name Address ID/FEI Business Operations The Estee Lauder Inc 802599436 manufacture(64141-014)
