SHISEIDO SUN PROTECTION LIP TREATMENT description, usages, side effects, indications, overdosage, supplying and lots more!

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SHISEIDO SUN PROTECTION LIP TREATMENT

SHISEIDO AMERICA INC.

SHISEIDO SUN PROTECTION LIP TREATMENT


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

ACTIVE INGREDIENTS: Purpose
OCTINOXATE 7.4% Sunscreen
TITANIUM DIOXIDE 4.5% Sunscreen

Use

  • helps prevent sunburn

Warnings

Skin Cancer/Skin Aging Alert

Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

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
  • children under 6 months: Ask a doctor

Inactive Ingredients

TRIETHYLHEXANOIN, POLYGLYCERYL-2 TRIISOSTEARATE, TRIISOSTEARIN, HYDROGENATED POLYISOBUTENE, POLYETHYLENE, PEG/PPG-36/41 DIMETHYL ETHER, MICROCRYSTALLINE WAX, STEARYL GLYCYRRHETINATE, GLUTATHIONE, ZINC MYRISTATE, THIOTAURINE, SODIUM ACETYLATED HYALURONATE, ALUMINUM HYDROXIDE, TOCOPHEROL, DIISOSTEARYL MALATE, SODIUM MAGNESIUM SILICATE, GLYCERIN, BHT, FRAGRANCE,

SHISEIDO SUN PROTECTION LIP TREATMENT Other information

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

Questions or comments?

Call toll free 1-800-906-7503

PRINCIPAL DISPLAY PANEL - 4g Cartridge Carton

SHISEIDO

SPF 35

Sun Protection
Lip Treatment

SUNSCREEN

4g NET WT. .14 OZ.

SHISEIDO SUN PROTECTION LIP TREATMENT

SHISEIDO SUN PROTECTION LIP TREATMENT

OCTINOXATE and TITANIUM DIOXIDE LIPSTICK

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52686-642
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 296 mg
titanium dioxide 180 mg

Inactive Ingredients

Ingredient Name Strength
TRIETHYLHEXANOIN
TRIISOSTEARIN
HYDROGENATED POLYBUTENE (1300 MW)
HIGH DENSITY POLYETHYLENE
PEG/PPG-36/41 DIMETHYL ETHER
MICROCRYSTALLINE WAX
STEARYL GLYCYRRHETINATE
GLUTATHIONE
ZINC MYRISTATE
THIOTAURINE
aluminum hydroxide
.ALPHA.-TOCOPHEROL
Diisostearyl Malate
GLYCERIN
BUTYLATED HYDROXYTOLUENE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 4 in 1 CARTRIDGE
2 NDC:52686-642-20 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-10-01


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