CLE DE PEAU BEAUTE description, usages, side effects, indications, overdosage, supplying and lots more!

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CLE DE PEAU BEAUTE

SHISEIDO CO., LTD.

Cle de peau Beaute Powder Foundation


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
OCTINOXATE 1.9% Sunscreen
TITANIUM DIOAXIDE 15.0% Sunscreen

CLE DE PEAU BEAUTE Uses

  • helps prevent sunburn
  • higher SPF gives more sunburn protection

Warnings

For external use only

When using this product

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

Stop use and ask a doctor if

  • rash or irritation develops and lasts.

Keep out of reach of children.

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

Directions

  • apply evenly before sun exposure and as needed
  • children under 6 months of age: ask a doctor

Inactive ingredients

TALC, SYNTHETIC FLUORPHLOGOPITE, BARIUM SULFATE, DIMETHICONE, TRIETHYLHEXANOIN, BIS-BEHENYL/PHYTOSTERYL DIMER DILINOLEATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, SILICA, NYLON-12, SILICA DIMETHYL SILYLATE, TOCOPHERYL ACETATE, PRUNUS SPECIOSA LEAF EXTRACT, SODIUM ACETYLATED HYALURONATE, ROSA ROXBURGHII FRUIT EXTRACT CAMELLIA SINENSIS LEAF EXTRACT, SORBITAN SESQUIISOSTEARATE, TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL HEXYL DIMETHICONE, METHICONE, ALUMINUM HYDROXIDE, ALUMINUM DISTEARATE, TRIETHOXYSILYLETHYL POLYDIMETHYLSILOXYETHYL DIMETHICONE, SODIUM MAGNESIUM SILICATE, POLYSILICONE-2, GLYCERIN, TOCOPHEROL, WATER, BUTYLENE GLYCOL, ALCOHOL, BHT, CHLORPHENESIN, FRAGRANCE, MICA, ZINC OXIDE, IRON OXIDES

Questions ?

1-800-906-7503

PRINCIPAL DISPLAY PANEL - 11g Carton

clé de peau
BEAUTÉ

powder foundation

SPF 21
sunscreen

11g NET WT. .38 OZ.

CLE DE PEAU BEAUTE

CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-300
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-300-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-301
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-301-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-302
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-302-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-303
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-303-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-304
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-304-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-305
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-305-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-306
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-306-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


CLE DE PEAU BEAUTE

Octinoxate and Titanium dioxide POWDER

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-307
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 209 mg
titanium dioxide 1.65 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 11 in 1 TRAY
2 NDC:52685-307-30 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-09-01


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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