FDA.reportPublic FDA data

Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 5N Neutral

Manufacturer
Parfums Christian Dior
Effective date
2026-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-03 03:03:02

Label at a glance#

ProductDior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 5N Neutral
Active ingredientOCTISALATE, TITANIUM DIOXIDE
Label structure7 sections

Indications and uses

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.

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, especially fr...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octisalate 4.50%
Titanium dioxide 1.41%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

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

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.
  • 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

AQUA (WATER) • DICAPRYLYL CARBONATE • GLYCERIN • SILICA • UNDECANE • POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE • ALCOHOL • PROPANEDIOL • CELLULOSE • DIPROPYLENE GLYCOL • POLYGLYCERYL-3 DIISOSTEARATE • C9-12 ALKANE • TRIDECANE • LECITHIN • HYDROXYPROPYL STARCH • PARFUM (FRAGRANCE) • STEARALKONIUM HECTORITE • DEXTRIN ISOSTEARATE • SODIUM MYRISTOYL GLUTAMATE • COCO-CAPRYLATE/CAPRATE • SODIUM CITRATE • SODIUM BENZOATE • SORBITAN SESQUIISOSTEARATE • PROPYLENE CARBONATE • OCTYLDODECANOL • MICA • CITRIC ACID • ALUMINUM HYDROXIDE • ALUMINA • STEARIC ACID • TOCOPHEROL • DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER • PENTYLENE GLYCOL • COLLAGEN AMINO ACIDS.

MAY CONTAIN: CI 77163 (BISMUTH OXYCHLORIDE) • CI 77491 (IRON OXIDES) • CI 77492 (IRON OXIDES) • CI 77499 (IRON OXIDES) • CI 77891 (TITANIUM DIOXIDE) • CI 77947 (ZINC OXIDE)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer label19Outer label19Box19Box19Inner label19Inner label19

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61957-371861957-3718-0

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
DICAPRYLYL CARBONATE609A3V1SUAIACT
GLYCERINPDC6A3C0OXIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
UNDECANEJV0QT00NUEIACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
ALCOHOL3K9958V90MIACT
PROPANEDIOL5965N8W85TIACT
POWDERED CELLULOSESMD1X3XO9MIACT
DIPROPYLENE GLYCOLE107L85C40IACT
POLYGLYCERYL-3 DIISOSTEARATE46P231IQV8IACT
C9-12 ALKANE7J5R5W72QMIACT
TRIDECANEA3LZF0L939IACT
HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT)9M44R3409AIACT
STEARALKONIUM HECTORITEOLX698AH5PIACT
SODIUM MYRISTOYL GLUTAMATEAYU7QD893WIACT
COCOYL CAPRYLOCAPRATE8D9H4QU99HIACT
SODIUM CITRATE, UNSPECIFIED FORM1Q73Q2JULRIACT
SODIUM BENZOATEOJ245FE5EUIACT
SORBITAN SESQUIISOSTEARATEVU97D01BF9IACT
PROPYLENE CARBONATE8D08K3S51EIACT
OCTYLDODECANOL461N1O614YIACT
MICAV8A1AW0880IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
ALUMINUM OXIDELMI26O6933IACT
STEARIC ACID4ELV7Z65APIACT
TOCOPHEROLR0ZB2556P8IACT
PENTYLENE GLYCOL50C1307PZGIACT
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
Dior Backstage Glow-Up Skin Tint Tinted Moisturizer SPF 20 5N NeutralOCTISALATE, TITANIUM DIOXIDEParfums Christian Diorc981ae5e-e7e8-484b-b682-fb96d501e03b2026-05-06WarningsExact identifier
ndc (package): 61957-3718-0
ndc (product): 61957-3718
ndc11 (package): 61957371800
spl id: 50af0497-e8df-4d08-e063-6394a90a936d
spl set id: c981ae5e-e7e8-484b-b682-fb96d501e03b

Reported adverse events (FAERS/openFDA)#

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