SUN PROTECTION BODY SUNSCREEN BROAD SPECTRUM SPF 30 LA PRAIRIE- avobenzone, homosalate, octisalate, oxybenzone lotion

Sun Protection Body Sunscreen Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Sun Protection Body Sunscreen Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by Temmentec Ag. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients        Purpose

Avobenzone 3.0%          Sunscreen

Homosalate 7.0 %          Sunscreen

Octisalate 5.0%              Sunscreen

Oxybenzone 5.0%          Sunscreen

Uses

helps prevent sunburn

warning

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

indications

Stop use and ask a doctor if rash occurs.

warnings

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.

Directions

  apply daily after cleansing and toning

  smooth over body

  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 increases 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, Undecrylene Dimethicone, Polyester-8, Polyglyceryl-3 Methylglucose Distearate, Butylene Glycol, Pentylene Glycol, Steareth-21, Glycoproteins, Panax Ginseng Root Extract, Equisetum Arvense (Horsetail) Extract, Sodium Hyaluronate, Octyldodecyl Olivate, Allantoin, Porphyra Umbilicalis Extract, Tocopheryl Acetate, Benzylidene Dimethoxydimethylindanone, Sea Water (Maris Aqua), Diethylhexyl Syringyldenemalonate, Polyacrylamide, Pelvetia Canaliculata Extract, Lecithin, Caprylic/Capric Triglyceride, Palmaria Palmata Extract, Ethylhexylglycerin, Algae Extract, Steareth-2, Disodium EDTA, Hydroxypropyl Starch Phosphate, Alcohol, C13-14 Isoparaffin, Sodium Lactate, Stearyl Alcohol, Dipropylene Glycol, Laureth-7, Fragrance (Parfum), Benzyl Alcohol, Phenoxyethanol, Chlorphenesin, Methylparaben, Propylparaben

display panel

Sun Protection Lotion Body

Lotion Solaire Protectrice Corps

Sunscreen Broad Spectrum SPF 30

La Prairie Switzerland

180 ml/ 6.0 Fl. Oz.

Made in Switzerland - Fabrique en Suisse

INGREDIENTS AND APPEARANCE

SUN PROTECTION BODY SUNSCREEN BROAD SPECTRUM SPF 30  LA PRAIRIE
avobenzone, homosalate, octisalate, oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68807-308
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3.0 g  in 100 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	7.0 g  in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5.0 g  in 100 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	5.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
DIMETHICONE (UNII: 92RU3N3Y1O)
POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
STEARETH-21 (UNII: 53J3F32P58)
ASIAN GINSENG (UNII: CUQ3A77YXI)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALLANTOIN (UNII: 344S277G0Z)
PORPHYRA UMBILICALIS (UNII: 14AN0J70WO)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BENZYLIDENE DIMETHOXYDIMETHYLINDANONE (UNII: 75HIF3C97L)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
PELVETIA CANALICULATA (UNII: 8U1M44KESN)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
DULSE (UNII: 7832HOY4ZQ)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
STEARETH-2 (UNII: V56DFE46J5)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALCOHOL (UNII: 3K9958V90M)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
SODIUM LACTATE (UNII: TU7HW0W0QT)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
LAURETH-7 (UNII: Z95S6G8201)
BENZYL ALCOHOL (UNII: LKG8494WBH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CHLORPHENESIN (UNII: I670DAL4SZ)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68807-308-02	1 in 1 CARTON
1	NDC: 68807-308-01	180 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	04/05/2013

Labeler - Temmentec Ag (480586411)

Registrant - Temmentec Ag (480586411)

Establishment
Name	Address	ID/FEI	Business Operations
Temmentec Ag		480586411	manufacture(68807-308)