SUN PROTECTION FACE SUNSCREN BROAD SPECTRUM SPF 30 description, usages, side effects, indications, overdosage, supplying and lots more!

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SUN PROTECTION FACE SUNSCREN BROAD SPECTRUM SPF 30

La Prairie, Inc.

SUN PROTECTION EMULSION FACE SUNSCREN BROAD SPECTRUM SPF 30


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

  • Avobenzone 3.0%
    Homosalate 10.0%
    Octisalate 2.6%
    Octocrylene 2.4%
    Oxybenzone 5.0%

Purpose

Sunscreen

SUN PROTECTION FACE SUNSCREN BROAD SPECTRUM SPF 30 Uses

• helps prevent sunburn

Warnings

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:

• apply daily after cleansing and toning • smooth over face and throat • apply liberally 15 minutes before sun exposure • children under 6 months of age: Ask a doctor • reapply at least every 2 hours • use a water resistant sunscreen if swimming or sweating • Sun Protection Measures. Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: • Limit time in the sun, especially from 10 a.m. - 2 p.m. • Wear long-sleeve shirts, pants, hats and sunglasses

Inactive Ingredients:

Water (Aqua), Caprylyl Methicone, Hexyldecanol, Dimethicone, Polyglyceryl-3 Methylglucose Distearate, Undercrylene Dimethicone, Aluminium Stearch Octenylsuccinate, Steareth-21, Octyldodecyl Olivate, Cetyl Alcohol, Silica, Glycerin, Glycoproteins*, Panax Ginseng Root Extract*, Equisetum Arvense (Horsetail) Extract*, Sodium Hyaluronate, Corallina Officinalis Extract, Sea Water (Maris Aqua), Algae Extract, Aloe Barbadensis Leaf juice, Steareth-2, Ethylhexyl Glycerin, Disodium EDTA, Benzylidene Dimethoxydimethylidanone, Sodium Hydroxide, Porphyra  Umbilicalis Extract, Squalane, Carbomer, Potassium Sorbate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Palmaria Palmata Extract, Tocopheryl Acetate, Diethylhexyl Syringyldenemalonate, Pelvetia Canaliculata Extract, Polysorbate 60, Lecithin, Caprylic/Capric Triglyceride, Sodium Lactate, Caprylyl Glycol, Alcohol, Benzyl Alcohol, Fragrance (Parfum), Phenoxyethanol, Chlorphenesin, Sodium Benzoate, Methylparaben, Ethylparaben, Propylparaben (i7 1) * La Prairie's exclusive Cellular Complex US Patent 5.840.309

Other Information

• Protect the product in this container from excessive heat and direct sun

Questions or comments?

Call toll free 1-800-821-5718 or visit www.laprairie.com

LABORATOIRES LA PRAIRIE S.A.

CLARENS/MONTREUX • ZURICH D-76530 BADEN-BADEN MILANO • PARIS LA PRAIRIE, INC., DISTR. NEW YORK, N.Y. 10019

SUN PROTECTION EMULSION FACE SUNSCREEN BROAD SPECTRUM SPF 30 la prairie SWITZERLAND 125 ml e / 4.2 FL. OZ. MADE IN SWITZERLAND

Product Labels

SUN PROTECTION FACE SUNSCREN BROAD SPECTRUM SPF 30 SUN PROTECTION FACE SUNSCREN BROAD SPECTRUM SPF 30

SUN PROTECTION FACE SUNSCREN BROAD SPECTRUM SPF 30

AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE EMULSION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:68026-422
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 30 mg
HOMOSALATE Homosalate 100 mg
OCTISALATE OCTISALATE 26 mg
OCTOCRYLENE Octocrylene 24 mg
OXYBENZONE OXYBENZONE 50 mg

Inactive Ingredients

Ingredient Name Strength
water
Hexyldecanol
DIMETHICONE
ALUMINUM STARCH OCTENYLSUCCINATE
STEARETH-21
CETYL ALCOHOL
SILICON DIOXIDE
GLYCERIN
HYALURONATE SODIUM
CORALLINA OFFICINALIS
Aloe Vera Leaf
STEARETH-2
EDETATE DISODIUM
SQUALANE
POTASSIUM SORBATE
POLYSORBATE 60
MEDIUM-CHAIN TRIGLYCERIDES
sodium lactate
CAPRYLYL GLYCOL
ALCOHOL
BENZYL ALCOHOL
PHENOXYETHANOL
CHLORPHENESIN
SODIUM BENZOATE
METHYLPARABEN
ETHYLPARABEN
PROPYLPARABEN

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:68026-422-04 125 in 1 BOTTLE
2 NDC:68026-422-05 5 in 1 BOTTLE
3 NDC:68026-422-07 7 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-10-22


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