SHISEIDO BENEFIANCE WRINKLERESIST24 DAY description, usages, side effects, indications, overdosage, supplying and lots more!

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SHISEIDO BENEFIANCE WRINKLERESIST24 DAY

SHISEIDO AMERICA INC.

SHISEIDO BENEFIANCE WRINKLERESIST24 DAY CREAM


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
OCTINOXATE 4.9% Sunscreen
OCTOCRYLENE 5.0% Sunscreen

SHISEIDO BENEFIANCE WRINKLERESIST24 DAY 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 smoothly to face before sun exposure and as needed.
  • children under 6 months of age: ask a doctor.

Inactive Ingredients

WATER, GLYCERIN, DIPROPYLENE GLYCOL, BUTYLENE GLYCOL, PHENYL TRIMETHICONE, HYDROGENATED POLYDECENE, SORBITOL, MYRISTYL MYRISTATE, DIMETHICONE, SD ALCOHOL 40-B, PETROLATUM, STEARYL ALCOHOL, STEARIC ACID, SILICA, PALMITIC ACID, XANTHAN GUM, PEG/PPG-17/4 DIMETHYL ETHER, PHYTOSTERYL MACADAMIATE, TOCOPHERYL ACETATE, SAPINDUS MUKUROSSI PEEL EXTRACT, UNCARIA GAMBIR EXTRACT, SODIUM ACETYLATED HYALURONATE, HYDROXYPROLINE , THYMUS SERPILLUM EXTRACT, CHLORELLA VULGARIS EXTRACT, PEG-5 GLYCERYL STEARATE, GLYCERYL STEARATE SE, BUTYL METHOXYDIBENZOYLMETHANE, BENTONITE, TRISODIUM EDTA, POTASSIUM HYDROXIDE, SODIUM METAPHOSPHATE, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, ALCOHOL, SODIUM METABISULFITE, BHT, TOCOPHEROL, PHENOXYETHANOL, FRAGRANCE, IRON OXIDES

Questions?

1-800-906-7503

PRINCIPAL DISPLAY PANEL - 50mL Carton

SHISEIDO

BENEFIANCE
WrinkleResist24

Day Cream
SPF 15 • PA++
SUNSCREEN

50mL NET WT. 1.8 OZ.

SHISEIDO BENEFIANCE WRINKLERESIST24 DAY

SHISEIDO BENEFIANCE WRINKLERESIST24 DAY

Octinoxate and Octocrylene CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52686-230
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 2.51125 g
OCTOCRYLENE Octocrylene 2.5625 g

Inactive Ingredients

Ingredient Name Strength
water
GLYCERIN
DIPROPYLENE GLYCOL
BUTYLENE GLYCOL
PHENYL TRIMETHICONE
sorbitol
MYRISTYL MYRISTATE
DIMETHICONE
petrolatum
stearyl alcohol
STEARIC ACID
SILICON DIOXIDE
PALMITIC ACID
GLYCERYL MONOSTEARATE
AVOBENZONE
BENTONITE
PHENOXYETHANOL
EDETATE TRISODIUM
XANTHAN GUM
POTASSIUM HYDROXIDE
SODIUM POLYMETAPHOSPHATE
.ALPHA.-TOCOPHEROL ACETATE, DL-
ALCOHOL
SODIUM METABISULFITE
ferric oxide red
FERRIC OXIDE YELLOW
BUTYLATED HYDROXYTOLUENE
HYDROXYPROLINE
CHLORELLA VULGARIS
ALPHA-TOCOPHEROL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 51.25 in 1 JAR
2 NDC:52686-230-50 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2011-02-01


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