SHISEIDO WHITE LUCENT description, usages, side effects, indications, overdosage, supplying and lots more!

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SHISEIDO WHITE LUCENT

SHISEIDO AMERICA INC.

SHISEIDO WHITE LUCENT BRIGHTENING PROTECTIVE EMULSION wSPF 15•PA++


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active ingredients Purpose
OCTINOXATE 4.9% Sunscreen
OCTOCRYLENE 5.0% Sunscreen

SHISEIDO WHITE LUCENT 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, SD ALCOHOL 40-B, DIMETHICONE, SILICA, DIISOPROPYL SEBACATE, TRANEXAMIC ACID, HYDROGENATED POLYISOBUTENE, EUPHORBIA CERIFERA (CANDELILLA) WAX, PEG/PPG-14/7 DIMETHYL ETHER, ERYTHRITOL, PEG/PPG-17/4 DIMETHYL ETHER, 2-O-ETHYL ASCORBIC ACID, XANTHAN GUM GLUCOSYL HESPERIDIN, PHYTOSTERYL/OCTYLDODECYL LAUROYL GLUTAMATE, SODIUM HYALURONATE, BUTYL METHOXYDIBENZOYLMETHANE PEG/PPG-19/19 DIMETHICONE, BEHENYL ALCOHOL, PPG-8-CETETH-20, BEHENETH-20, TRISODIUM EDTA, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, STEARYL ALCOHOL, POTASSIUM HYDROXIDE, HYDROXYPROPYLCELLULOSE, BHT, POLYSILICONE-2, SODIUM METABISULFITE, TOCOPHEROL, PHENOXYETHANOL, FRAGRANCE, TITANIUM DIOXIDE, IRON OXIDES

Questions?

1-800-906-7503

SHISEIDO AMERICA INC.
NEW YORK, N.Y. 10022
MADE IN U.S.A.
SHISEIDO DIST.
NEW YORK • PARIS • MILANO
GLO. 10393

www.shiseido.com

PRINCIPAL DISPLAY PANEL - 75 mL Carton

SHISEIDO

WHITE LUCENT

Brightening
Protective Emulsion w
SPF 15 • PA++
SUNSCREEN

75mL 2.5 FL. OZ.

SHISEIDO WHITE LUCENT

SHISEIDO WHITE LUCENT

Octinoxate and Octocrylene EMULSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52686-228
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 3.479 g
OCTOCRYLENE Octocrylene 3.55 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 71 in 1 BOTTLE, PUMP
2 NDC:52686-228-10 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2010-02-01


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