FDA.reportPublic FDA data

OCTINOXATE

Manufacturer
Parfums Christian Dior
Effective date
2020-08-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:16:56

Label at a glance#

ProductDIORSKIN NUDE AIR LUMINIZER Fluide Illuminateur Bonne Mine Naturelle Healthy Glow Liquid Luminizer with Sunscreen Bro...
Active ingredientOCTINOXATE
Label structure7 sections

Indications and uses

Helps prevent sunburn.

Dosage and administration

Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating. Children under 6 months of age: ask a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.49%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn.

Warnings

WARNINGS SECTION

Skin Cancer/Skin Aging Alert: spending time in the sun increases your risk of skin cancer and early skin aging. this product has been show only to help prevent sunburn, not skin caner or early skin aging.

For external use only.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product,

OTC - WHEN USING SECTION

keep out of eyes.  Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun exposure.
  • Reapply at least every 2 hours
  • Use a water resistant sunscreen if swimming or sweating.
  • Children under 6 months of age: ask a doctor

Other Informations

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

TRISILOXANE, CYCLOPENTASILOXANE, ISODODECANE, DIPHENYL DIMETHICONE/VINYL DIPHENYL DIMETHICONE/SILSESQUIOXANE CROSSPOLYMER, PHENYL TRIMETHICONE, MICA, ALCOHOL, DIMETHICONE, PEG-10 DIMETHICONE, ACRYLATES/DIMETHICONE COPOLYMER, DISTEARDIMONIUM HECTORITE, OXIDIZED CORN OIL, VACCINIUM MACROCARPON (CRANBERRY) SEED OIL, AQUA (WATER), PHENOXYETHANOL, TRIETHOXYCAPRYLYLSILANE, PARFUM (FRAGRANCE), SILICA, TOCOPHERYL ACETATE, LINALOOL, HEXYL CINNAMAL, BHT, CITRONELLOL, TOCOPHEROL, ALPHA-ISOMETHYLIONONE, COUMARIN, HELIANTHUS AN- NUUS (SUNFLOWER SEED OIL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, [MAY CONTAIN: CI 15850 (RED 6, RED 7, RED 7 LAKE), CI 73360 (RED 30, RED 30 LAKE) CI 77163 (BISMUTH OXYCHLORIDE), CI 77491, CI 77492, CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)] N 11210/Z

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LUMINIZERLUMINIZERDiorDior

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61957-261061957-2610-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
TRISILOXANE9G1ZW13R0GIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ISODODECANEA8289P68Y2IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
MICAV8A1AW0880IACT
ALCOHOL3K9958V90MIACT
DIMETHICONE92RU3N3Y1OIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
CRANBERRY SEED OIL73KDS3BW5EIACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
LINALOOL, (+/-)-D81QY6I88EIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
TOCOPHEROLR0ZB2556P8IACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
COUMARINA4VZ22K1WTIACT
SUNFLOWER OIL3W1JG795YIIACT
ROSEMARYIJ67X351P9IACT
OCTINOXATE4Y5P7MUD51ACTIB

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
adc8e090-a804-550a-e053-2995a90a963c1422e9cb-6ba1-4792-9bfc-bd91ea8b47182020-08-26WarningsExact identifier
spl id: adc8e090-a804-550a-e053-2995a90a963c
spl set id: 1422e9cb-6ba1-4792-9bfc-bd91ea8b4718

Reported adverse events (FAERS/openFDA)#

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