FDA.reportPublic FDA data

Bright future skin tint SPF 25 35 bronze

Manufacturer
S+
Effective date
2024-12-02
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 20:47:46

Label at a glance#

ProductBright future skin tint SPF 25 35 bronze
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure8 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  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 value 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-sleeved shirts, pants,...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 7.49%

Titanium Dioxide 2.28%

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 ues 

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 
  • 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 value 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-sleeved 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 (AQUA), CYCLOPENTASILOXANE, GLYCERIN, ISODODECANE, PENTYLENE GLYCOL, ALCOHOL, DIMETHICONE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PEG-10 DIMETHICONE, XANTHAN GUM, SORBITAN SESQUIOLEATE, DISTEARDIMONIUM HECTORITE, PHENOXYETHANOL, ACRYLATES/DIMETHICONE COPOLYMER, ALUMINUM HYDROXIDE, ISOSTEARIC ACID, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, BUTYLENE GLYCOL, POLYHYDROXYSTEARIC ACID, SODIUM MYRISTOYL GLUTAMATE, SILICA SILYLATE, PROPYLENE CARBONATE, STEARIC ACID, HYDROLYZED RICE PROTEIN, SODIUM METABISULFITE, BHT, SHEA (BUTYROSPERMUM PARKII) SEEDCAKE EXTRACT, LEMON (CITRUS LIMON) FRUIT EXTRACT, TOCOPHEROL, TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77492), IRON OXIDES (CI 77491), IRON OXIDES (CI 77499).

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label9Label9

Inner Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BronzeBronze

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
31720-70931720-709-17

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
WATER059QF0KO0RIACT
CYCLOMETHICONE 50THT5PCI0RIACT
GLYCERINPDC6A3C0OXIACT
ISODODECANEA8289P68Y2IACT
PENTYLENE GLYCOL50C1307PZGIACT
ALCOHOL3K9958V90MIACT
DIMETHICONE92RU3N3Y1OIACT
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
XANTHAN GUMTTV12P4NEEIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
ISOSTEARIC ACIDX33R8U0062IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SODIUM MYRISTOYL GLUTAMATEAYU7QD893WIACT
PROPYLENE CARBONATE8D08K3S51EIACT
STEARIC ACID4ELV7Z65APIACT
SODIUM METABISULFITE4VON5FNS3CIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
TOCOPHEROLR0ZB2556P8IACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT
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
2856e188-e702-3c74-e063-6394a90aaeb32ba5a73f-e2a9-43d2-b857-5bbdfd6d579f2024-12-02WarningsExact identifier
spl id: 2856e188-e702-3c74-e063-6394a90aaeb3
spl set id: 2ba5a73f-e2a9-43d2-b857-5bbdfd6d579f

Reported adverse events (FAERS/openFDA)#

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