La Prairie Switzerland

Manufacturer
Temmentec Ag
Effective date
2010-05-25
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:08:33

Label at a glance#

ProductLa Prairie Switzerland Cellular Radiance Emulsion
Active ingredientAVOBENZONE, OCTINOXATE, OCTISALATE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients                        Purpose

Avobenzone 3.0%                        Sunscreen

Octinoxate 7.5%                          Sunscreen

Octisalate  5.0%                        Sunscreen

WARNINGS SECTION

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

-do not use on infants under 6 months of age

INDICATIONS & USAGE SECTION

Uses

-helps prevent sunburn

-for skin that burns easily

-provides moderate protection against sunburn

-higher SPF gives more sunburn protection


Directions

-for external use only

-when using this product keep out of eyes

-rinse with water to remove

-stop use and ask doctor if rash or irritation develops and lasts

-keep out of reach of children

-do not use on infants under 6 months of age

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), C12-15 Alkyl Ethylhexanoate, Cetyl Alcohol, Glycerin, Helianthus Annuus (Sunflower) Seed Oil, Sea Water (Maris Aqua), Dimethicone, Behenyl Alcohol, Stearyl Alcohol, Butylene Glycol, Propylene Glycol, Caprylic/Capric Triglyceride, Cyclopentasiloxane, Batyl Alcohol, Glycoproteins, Panax Ginseng Root Extract, Equisetum Arvense (Horsetail) Extract, Phytosterols, Silicornia Herbacea Extract, Niacinamide, Hydrolyzed Oat Protein, Alpinia Galang Leaf Extract, Quartz, Disodium Adenosine Triphosphate, Tocopherol, Carica Papaya (Papaya) Fruit Extract, Cholesteryl Nonanoate, Cimicifuga Racemosa Root Extract, Copper Gluconate, PEG-20 Phytosterol, Actinidia Polygama Fruit Extract, Acetyl Heptapeptide-Gold, Cholesteryl Oleate, Dimethylmethoxy Chromanyl Palmitate, Corallina Officinalis Extract, Carbomer, Cholsteryl Stearate, Acrylates Copolymer, Boswellia Serrata Extract, Ammonium Acryloyldimethltaurate/Beheneth-25 Methacrylate Crosspolymer, Phormidium Persicinum Extract, Caprylyl Glycol, Dextran, Magnesium Asparate Glyceryl Stearate, Disodium EDTA, Xanthan Gum, BHT, Fragrance (Parfum), Linalool, Hexyl Cinnamal, Hydroxycitronellal, Alpha-Isomethyl Ionone, Geraniol, Citronellol, Benzyl Benzoate, Butylphenyl Methylpropional, Evernia Furfuracea (Treemoss) Extract, Eugenol, Benzyl Salicylate, Limonene, Phenoxyethanol, Sorbia Acid, Methylparaben, Mica, Titanium Dioxide (CI 77891), Red (CI 14700), Yellow 5 (CI 19140), Gold

image of backimage of back

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cellular Radiance Emulsion

SPF 30

50 ml / 1.7 Fl. Oz.

image of front labelimage of front label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68807-301-112019-10-21C16284748780-1956f9ecf-d782-621f-e053-dbdaa90a74adCellular Radiance Emulsion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68807-301-11La Prairie SwitzerlandCellular Radiance Emulsion78.4 kg in 1 DRUMCREAM78.42

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68807-301LA PRAIRIE SWITZERLAND CELLULAR RADIANCE EMULSION (AVOBENZONE, OCTINOXATE, OCTISALATE) CREAM [TEMMENTEC AG]2Legacy NDC, 1 package rows20100526_cd5beee7-d8f5-4e1c-b990-98db641a20a2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX2
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
OCTISALATEACTIVE INGREDIENT4X49Y0596W2
AVOBENZONEACTIVE MOIETYG63QQF2NOX2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
OCTISALATEACTIVE MOIETY4X49Y0596W2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68807-30168807-301-11

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
AVOBENZONEG63QQF2NOXACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
34f18c0f-1669-44f9-b200-2bededba9ec5cd5beee7-d8f5-4e1c-b990-98db641a20a22010-05-25WarningsExact identifier
spl id: 34f18c0f-1669-44f9-b200-2bededba9ec5
spl set id: cd5beee7-d8f5-4e1c-b990-98db641a20a2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.