FDA.reportPublic FDA data

Givenchy Photo Perfexion Fluid Foundation SPF 20 Perfect Suede Tint 6.5

Manufacturer
LVMH Fragrance Brands
Effective date
2019-10-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:08:09

Label at a glance#

ProductGivenchy Photo Perfexion Fluid Foundation SPF 20 Perfect Suede Tint 6.5
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure7 sections

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 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 of 15 or higher and other sun protection measures including:         •  limit time in the sun, especi...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 2.997%
Titanium Dioxide 3.16%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

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

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

OTC - STOP USE SECTION

if rash occurs

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact
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
  • 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 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-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

Water, Cyclopentasiloxane, PEG-9 Polydimethylsiloxyethyl Dimethicone, Isodecyl Neopentanoate, Pentylene Glycol, Saccharomyces/xylinum/black Tea Ferment, Butylene Glycol, Acrylates Copolymer, Silica, Cyclohexasiloxane, Acrylates / Dimethicone Copolymer, Butylene Glycol Dicaprylate/Dicaprate, Phenoxyethanol, Aluminum Hydroxide, Stearic Acid, Sorbitan Sesquioleate, Dimethicone Crosspolymer, Alumina, Glycerin, Sodium Myristoyl Glutamate, Hydroxyethylcellulose, Sodium Hyaluronate, Lecithin, Fragrance, Dimethicone, Sodium Citrate, Butylphenyl Methylpropional, Citric Acid, Artemisia Capillaris Flower Extract, BHT, Hedera Helix (Ivy) Extract, Potassium Sorbate, Geraniol, Biotin.    May Contain: Titanium Dioxide, Iron Oxides, Mica.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Carton1Carton1ShadeShadeBottle1Bottle1

Tester LabelTester Label

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60905-004960905-0049-1, 60905-0049-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CYCLOMETHICONE 50THT5PCI0RIACT
PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONETYP81E471FIACT
ISODECYL NEOPENTANOATEW60VYE24XCIACT
PENTYLENE GLYCOL50C1307PZGIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
CYCLOMETHICONE 6XHK3U310BAIACT
BUTYLENE GLYCOL DICAPRYLATE13P836X9Q6IACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
STEARIC ACID4ELV7Z65APIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
ALUMINUM OXIDELMI26O6933IACT
GLYCERINPDC6A3C0OXIACT
SODIUM MYRISTOYL GLUTAMATEAYU7QD893WIACT
HYALURONATE SODIUMYSE9PPT4THIACT
DIMETHICONE92RU3N3Y1OIACT
SODIUM CITRATE1Q73Q2JULRIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ARTEMISIA CAPILLARIS FLOWERKG4724BPZGIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
HEDERA HELIX LEAFZP9XFG71A7IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
GERANIOLL837108USYIACT
BIOTIN6SO6U10H04IACT
FERRIC OXIDE RED1K09F3G675IACT
MICAV8A1AW0880IACT
OCTINOXATE4Y5P7MUD51ACTIB
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
947befcf-af11-662e-e053-2a95a90a8254718edc9a-b214-4fce-b0e8-e59e8651d6852019-10-09WarningsExact identifier
spl id: 947befcf-af11-662e-e053-2a95a90a8254
spl set id: 718edc9a-b214-4fce-b0e8-e59e8651d685

Reported adverse events (FAERS/openFDA)#

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