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

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CLE DE PEAU BEAUTE SYNACTIF DAYTIME MOISTURIZER

SHISEIDO CO., LTD.

cle de peau BEAUTE SYNACTIF DAYTIME MOISTURIZER


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
ENSULIZOLE 2.0% Sunscreen
OCTINOXATE 4.9% Sunscreen

CLE DE PEAU BEAUTE SYNACTIF DAYTIME MOISTURIZER 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 generously before sun exposure and as needed.
  • apply and reapply as directed to avoid lowering protection.
  • apply to all skin exposed to the sun.
  • children under 6 months of age: ask a doctor

Inactive ingredients

WATER, GLYCERIN, BUTYLENE GLYCOL, CYCLOMETHICONE, DIPROPYLENE GLYCOL, SILICA, DIMETHICONE, TRIETHYLHEXANOIN, DIPHENYLSILOXY PHENYL TRIMETHICONE, BEHENYL ALCOHOL, BEHENETH-20, TRIETHANOLAMINE, METHYL AMINOMETHYLCYCLOHEXANE CARBOXAMIDE HCl, XANTHAN GUM, TOCOPHERYL ACETATE, SODIUM HYALURONATE, SODIUM ACETYLATED HYALURONATE, LAURYL BETAINE, BUPLEURUM FALCATUM ROOT EXTRACT, UNCARIA GAMBIR EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, STEARYL ALCOHOL, SODIUM METAPHOSPHATE, CELLULOSE GUM, TRISODIUM EDTA, ALUMINUM HYDROXIDE, ISOSTEARIC ACID, BHT, ALCOHOL, TOCOPHEROL, PHENOXYETHANOL, SODIUM BENZOATE, FRAGRANCE, TITANIUM DIOXIDE, IRON OXIDES

Questions?

1-800-906-7503

Distributed by
SHISEIDO COSMETICS (AMERICA) LTD.
NEW YORK, NY 10022

PRINCIPAL DISPLAY PANEL - 20mL Bottle Carton

SYNACTIF

Daytime moisturizer
SPF 17 sunscreen

20mL NET WT. .75 OZ.

CLE DE PEAU BEAUTE SYNACTIF DAYTIME MOISTURIZER

CLE DE PEAU BEAUTE SYNACTIF DAYTIME MOISTURIZER

Ensulizole and Octinoxate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52685-380
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
Ensulizole Ensulizole 430 mg
OCTINOXATE OCTINOXATE 1054 mg

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
BUTYLENE GLYCOL
cyclomethicone
DIPROPYLENE GLYCOL
SILICON DIOXIDE
TRIETHYLHEXANOIN
DIMETHICONE
docosanol
titanium dioxide
TROLAMINE
stearyl alcohol
PHENOXYETHANOL
XANTHAN GUM
SODIUM POLYMETAPHOSPHATE
CARBOXYMETHYLCELLULOSE SODIUM
.ALPHA.-TOCOPHEROL ACETATE, DL-
EDETATE TRISODIUM
aluminum hydroxide
HYALURONATE SODIUM
ferric oxide red
FERRIC OXIDE YELLOW
isostearic acid
BUTYLATED HYDROXYTOLUENE
LAURYL BETAINE
ALCOHOL
.ALPHA.-TOCOPHEROL
BUPLEURUM FALCATUM ROOT
GREEN TEA LEAF
SODIUM BENZOATE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 21.52 in 1 BOTTLE
2 NDC:52685-380-10 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-11-01


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