FDA.reportPublic FDA data

SEPHORA ROUGE BALM SUNSCREEN SPF20 B09-Mild Plum

Manufacturer
INTERCOS EUROPE SPA | Intercos Europe S.p.A.
Effective date
2019-12-12
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:52:13

Label at a glance#

ProductSEPHORA ROUGE BALM SUNSCREEN SPF20 B09-Mild Plum
Active ingredientOCTINOXATE, OCTISALATE, TITANIUM DIOXIDE
Label structure1 sections

Label contents#

Full prescribing information#

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Inner packageInner packageOuterOuter

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63272-50863272-508-16

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIISOSTEARYL MALATEQBS8A3XZGQIACT
OCTYLDODECANOL461N1O614YIACT
ISOSTEARYL ISOSTEARATEIV0Z586Z4YIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
ANHYDROUS DIBASIC CALCIUM PHOSPHATEL11K75P92JIACT
DIPENTAERYTHRITYL HEXAHYDROXYSTEARATE74J1X57U42IACT
MICAV8A1AW0880IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
ALCOHOL3K9958V90MIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE)255PIF62MSIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
WATER059QF0KO0RIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
CITRUS JUNOS FRUIT RINDR13K440UHYIACT
ETHYLHEXYL PALMITATE2865993309IACT
SILICA DIMETHYL SILYLATEEU2PSP0G0WIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CAPRYLYL GLYCOL00YIU5438UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
HYALURONATE SODIUMYSE9PPT4THIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c23b53a8-80cb-8603-e053-2a95a90a2290029c3295-90ff-4af0-a456-33f736a1e6302021-05-13Exact identifier
spl set id: 029c3295-90ff-4af0-a456-33f736a1e630

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.