BRIGHT FUTURE SKIN TINT SPF 25 11 IVOIRE PUR PURE- octinoxate, titanium dioxide cream 
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Bright future skin tint SPF 25 11 ivoire pur pure

Drug Facts

Active ingredient

Octinoxate 7.49%

Titanium Dioxide 2.28%

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not ues 

  • on damaged or broken skin

When using this product 

  • keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if

  • rash occurs

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

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:

Label2

Inner Label

Ivoire Pur

BRIGHT FUTURE SKIN TINT SPF 25 11 IVOIRE PUR PURE 
octinoxate, titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:31720-702
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE74.9 mg  in 1 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE22.8 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
XANTHAN GUM (UNII: TTV12P4NEE)  
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SODIUM MYRISTOYL GLUTAMATE (UNII: AYU7QD893W)  
PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
TOCOPHEROL (UNII: R0ZB2556P8)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
WATER (UNII: 059QF0KO0R)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISODODECANE (UNII: A8289P68Y2)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
ALCOHOL (UNII: 3K9958V90M)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:31720-702-171 in 1 CARTON08/28/2017
125 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02008/28/2017
Labeler - S+ (572406531)

Revised: 12/2023
Document Id: 0d9cfb04-5c52-9b9c-e063-6394a90a1d28
Set id: 8c7fb53c-9993-4505-bf2a-c3e07e38d987
Version: 3
Effective Time: 20231228
 
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