SHISEIDO WHITE LUCENT BRIGHTENING SPOT-CONTROL BASE UV IVORY

Dosage form: paste
Ingredients: OCTINOXATE 0.9396g in 32.4g, TITANIUM DIOXIDE 2.7216g in 32.4g
Labeler: SHISEIDO AMERICA INC.
NDC Code: 52686-249

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

SHISEIDO WHITE LUCENT BRIGHTENING SPOT-CONTROL BASE UV

Drug Facts

ACTIVE INGREDIENTS:Purpose
OCTINOXATE 2.9%Sunscreen
TITANIUM DIOXIDE 8.4%Sunscreen

Use
  • helps prevent sunburn

Warnings

For external use only

Do not use 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 product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

For sunscreen use:

  • apply liberally 15 minutes before sun exposure
  • use a water resistant sunscreen if swimming or sweating
  • 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 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: Ask a doctor

Inactive Ingredients

CYCLOMETHICONE, WATER, SD ALCOHOL 40-B, BUTYLENE GLYCOL, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PEG-10 DIMETHICONE, CETYL ETHYLHEXANOATE, TRANEXAMIC ACID, ALUMINUM HYDROXIDE, GLYCERIN, SORBITAN SESQUIISOSTEARATE, DISTEARDIMONIUM HECTORITE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PEG/PPG-14/7 DIMETHYL ETHER, 2-O-ETHYL ASCORBIC ACID, SODIUM HYALURONATE, STEARIC ACID, ISOSTEARIC ACID, ALUMINUM DISTEARATE, TRISODIUM EDTA, POLYSILICONE-2, SODIUM METABISULFITE, BHT, TOCOPHEROL, PHENOXYETHANOL, FRAGRANCE, TITANIUM DIOXIDE, IRON OXIDES, CHROMIUM HYDROXIDE GREEN,

Other information
  • protect this product in this container from excessive heat and direct sun.

Questions or comments?

Call toll free 1-800-906-7503

SHISEIDO AMERICA INC.
NEW YORK, N.Y. 10022
SHISEIDO DIST. NEW YORK • PARIS • MILANO

PRINCIPAL DISPLAY PANEL - 30mL Tube Carton - IVORY

SHISEIDO

WHITE LUCENT

Brightening
Spot-Control
Base UV

BROAD SPECTRUM
SPF 37

SUNSCREEN

30mL NET WT. 1.1 OZ.

PRINCIPAL DISPLAY PANEL - 30mL Tube Carton - GREEN

SHISEIDO

WHITE LUCENT

Brightening
Spot-Control
Base UV

BROAD SPECTRUM
SPF 37

SUNSCREEN

30mL NET WT. 1.1 OZ.

PRINCIPAL DISPLAY PANEL - 30mL Tube Carton - PINK

SHISEIDO

WHITE LUCENT

Brightening
Spot-Control
Base UV

BROAD SPECTRUM
SPF 37

SUNSCREEN

30mL NET WT. 1.1 OZ.

SHISEIDO WHITE LUCENT   BRIGHTENING SPOT-CONTROL BASE UV IVORY
octinoxate and titanium dioxide paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52686-249
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE0.9396 g  in 32.4 g
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE2.7216 g  in 32.4 g
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 
WATER 
TITANIUM DIOXIDE 
BUTYLENE GLYCOL 
PEG-10 DIMETHICONE (600 CST) 
CETYL ETHYLHEXANOATE 
TRANEXAMIC ACID 
ALUMINUM HYDROXIDE 
GLYCERIN 
STEARIC ACID 
FERRIC OXIDE RED 
FERRIC OXIDE YELLOW 
ISOSTEARIC ACID 
PHENOXYETHANOL 
ALUMINUM DISTEARATE 
EDETATE TRISODIUM 
2-O-ETHYL ASCORBIC ACID 
SODIUM METABISULFITE 
BUTYLATED HYDROXYTOLUENE 
HYALURONATE SODIUM 
.ALPHA.-TOCOPHEROL 
Packaging
#Item CodePackage Description
1NDC:52686-249-601 TUBE in 1 CARTON
132.4 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35202/01/2011
SHISEIDO WHITE LUCENT   BRIGHTENING SPOT-CONTROL BASE UV GREEN
octinoxate and titanium dioxide paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52686-250
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE0.9396 g  in 32.4 g
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE2.7216 g  in 32.4 g
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 
WATER 
TITANIUM DIOXIDE 
BUTYLENE GLYCOL 
PEG-10 DIMETHICONE (600 CST) 
CETYL ETHYLHEXANOATE 
TRANEXAMIC ACID 
ALUMINUM HYDROXIDE 
GLYCERIN 
STEARIC ACID 
FERRIC OXIDE RED 
FERRIC OXIDE YELLOW 
ISOSTEARIC ACID 
PHENOXYETHANOL 
ALUMINUM DISTEARATE 
EDETATE TRISODIUM 
2-O-ETHYL ASCORBIC ACID 
SODIUM METABISULFITE 
BUTYLATED HYDROXYTOLUENE 
HYALURONATE SODIUM 
.ALPHA.-TOCOPHEROL 
Packaging
#Item CodePackage Description
1NDC:52686-250-601 TUBE in 1 CARTON
132.4 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35202/01/2011
SHISEIDO WHITE LUCENT   BRIGHTENING SPOT-CONTROL BASE UV PINK
octinoxate and titanium dioxide paste
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52686-251
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (OCTINOXATE) OCTINOXATE0.9396 g  in 32.4 g
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE2.7216 g  in 32.4 g
Inactive Ingredients
Ingredient NameStrength
CYCLOMETHICONE 
WATER 
TITANIUM DIOXIDE 
BUTYLENE GLYCOL 
PEG-10 DIMETHICONE (600 CST) 
CETYL ETHYLHEXANOATE 
TRANEXAMIC ACID 
ALUMINUM HYDROXIDE 
GLYCERIN 
STEARIC ACID 
FERRIC OXIDE RED 
FERRIC OXIDE YELLOW 
ISOSTEARIC ACID 
PHENOXYETHANOL 
ALUMINUM DISTEARATE 
EDETATE TRISODIUM 
2-O-ETHYL ASCORBIC ACID 
SODIUM METABISULFITE 
BUTYLATED HYDROXYTOLUENE 
HYALURONATE SODIUM 
.ALPHA.-TOCOPHEROL 
Packaging
#Item CodePackage Description
1NDC:52686-251-601 TUBE in 1 CARTON
132.4 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35202/01/2011
Labeler - SHISEIDO AMERICA INC. (782677132)
Establishment
NameAddressID/FEIOperations
SHISEIDO AMERICA INC.782677132MANUFACTURE(52686-249, 52686-250, 52686-251), ANALYSIS(52686-249, 52686-250, 52686-251)
Establishment
NameAddressID/FEIOperations
Davlyn Industries Inc624436254MANUFACTURE(52686-249, 52686-250, 52686-251)

Revised: 06/2012
 
SHISEIDO AMERICA INC.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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