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, Chlosteryl 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 (14700), Yellow 5 (CI 19140), Gold

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cellular Radiance Emulsion

SPF 30

50 ml / 1.7 Fl. Oz.

image of front label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59614-301-02	2019-10-21	C162847	48780-1	956f9ecf-d776-621f-e053-dbdaa90a74ad	Cellular Radiance Emulsion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59614-301-01	La Prairie SwitzerlandCellular Radiance Emulsion	50 mL in 1 TUBE	CREAM	50		2
59614-301-02	La Prairie SwitzerlandCellular Radiance Emulsion	1 in 1 BOX	CREAM	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59614-301	LA PRAIRIE SWITZERLAND CELLULAR RADIANCE EMULSION (AVOBENZONE, OCTINOXATE, OCTISALATE) CREAM [JUVENA PRODUITS DE BEAUTE]	2	Legacy NDC, 2 package rows	20100508_0daa1d8f-4522-4a1a-9ebf-78907be6aa9d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
AVOBENZONE	ACTIVE INGREDIENT	G63QQF2NOX	2
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	2
OCTISALATE	ACTIVE INGREDIENT	4X49Y0596W	2
AVOBENZONE	ACTIVE MOIETY	G63QQF2NOX	2
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	2
OCTISALATE	ACTIVE MOIETY	4X49Y0596W	2

Products#

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

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

La Prairie Switzerland Cellular Radiance Emulsion
Avobenzone, Octinoxate, Octisalate
AVOBENZONE
OCTINOXATE
OCTISALATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59614-301	59614-301-01, 59614-301-02

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
Name	UNII	Kind
AVOBENZONE	G63QQF2NOX	ACTIB
OCTINOXATE	4Y5P7MUD51	ACTIB
OCTISALATE	4X49Y0596W	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
57da029e-b645-4e14-8bcf-659432050e0d			0daa1d8f-4522-4a1a-9ebf-78907be6aa9d	2010-05-07	Warnings	Exact identifier spl id: 57da029e-b645-4e14-8bcf-659432050e0d spl set id: 0daa1d8f-4522-4a1a-9ebf-78907be6aa9d

Reported adverse events (FAERS/openFDA)#

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