Octinoxate, Titanium dioxide, Zinc oxide

Manufacturer
Parfums Christian Dior
Effective date
2023-11-03
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:22:10

Label at a glance#

ProductCAPTURE DREAMSKIN FRESH AND PERFECT CUSHION WITH SUNSCREEN BROAD SPECTRUM SPF 50 040
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE
Label structure7 sections

Indications and uses

Helps prevent sunburn. If used as directed with other sun protection measures ( ), decreases the risk of skin cancer and early skin aging caused by the sun. see Directions

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. Spending time in the sun increases your risk of skin cancer and early skin aging. To decreases this risk, regularly use a sunsreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: Sun Protection Measures. limit time in the sun, especially fro...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.00%

Titanium dioxide 4.15%

Zinc oxide 9.80%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn.
  • If used as directed with other sun protection measures ( ), decreases the risk of skin cancer and early skin aging caused by the sun. see Directions

Warnings

WARNINGS SECTION

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.
  • Spending time in the sun increases your risk of skin cancer and early skin aging. To decreases this risk, regularly use a sunsreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: Sun Protection Measures.
  • limit time in the sun, especially from 10 a.m. - 2 p.m.
  • wear long-sleeve shirts, pants, hats, and sunglasses.
  • Children under 6 months of age: ask a doctor.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

AQUA (WATER), CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, PEG-10 DIMETHICONE, DIMETHICONE, BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE, PROPANEDIOL, LAURYL PEG-9 POLYDIMETHYLSILOXETHYL DIMETHICONE, HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER, TRISILOXANE, PHENYL TRIMETHICONE, GLYCERIN, SODIUM CHLORIDE, DIMETHICONE/PEG-/ CROSSPOLYMER, DISTEARDIMONIUM HECTORITE, ALUMINUM HYDROXIDE, PHENOXYETHANOL, STEARIC ACID, XYLITOL, POLYMETHYL METHACRYLATE, PARFUM (FRAGRANCE), CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, DISODIUM EDTA, SILICA, ZINC GLUCONATE, ADENOSINE, BUTYLPHENYL METHYLPROPIONAL, LIMONENE, SYNTHETIC FLUORPHLOGOPITE, PALMARIA PALMATA EXTRACT, SODIUM BENZOATE, ALPHA-ISOMETHYL IONONE, GERANIOL, BUTYLENE GLYCOL, JASMINUM OFFICINALE (JASMINE) FLOWER EXTRACT, ALCOHOL, HYDROGEN DIMETHICONE, BHT, SAPONINS, TOCOPHEROL, AFRAMOMUM ANGUSTIFOLIUM SEED EXTRACT. [MAY CONTAIN: CI 77491, CI 77492, CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)].

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

L1L1L2L2L3L3L4L4

Products#

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

DailyMed product names page 1 of 2 · 44 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61957-290561957-2905-0, 61957-2905-1

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 42 matching rows.

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
27d19a75-52b6-5dd9-e063-6394a90a326e3eebed9d-45e6-4ce8-9446-8e8d9a8b970e2024-11-26WarningsExact identifier
spl set id: 3eebed9d-45e6-4ce8-9446-8e8d9a8b970e

Reported adverse events (FAERS/openFDA)#

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