La Prairie Switzerland

Manufacturer
Juvena Produits de Beaute GMBH | Temmentec AG | Trichema AG
Effective date
2010-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:41

Label at a glance#

ProductLa Prairie Switzerland Cellular Blemish Control
Active ingredientSALICYLIC ACID
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Salicylic Acid    2.0%

WARNINGS SECTION

Warnings: For external use only. Avoid contact with eyes. Using topical acne medications with this product may result in increased dryness or irritation of the skin. If this occurs, discontinue use and consult a physician. Keep out of reach of children. Do not use on children.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: SD Alcohol 40-B (Alcohol Denat.), Water (Aqua), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Salicylic Acid, Glycerin, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Betula Alba (Birch) Bark Extract, Arctium Lappa (Burdock) Root Extract, Cupressus Sempervirens (Cypress) Seed Extract, Lamium Album (White Nettle) Flower Extract, Salvia Officinalis (Sage) Leaf Extract, Benzalkonium Chloride, PEG-8, Alpha-Glucan Oligosaccharide, Melia Azadirachta (Neem) Leaf Extract, Hydrolyzed Milk Protein, Glucose Oxidase, Lactoperoxidase, Lactoferrin, Potassium Thiocyanate, Glycoproteins, Panax Ginseng Root Extract, Equisetum Arvense (Horsetail) Extract, Glucose Pentaacetate, Lecithin, Caprylyl Glycol, Arvena Sativa (Oat) Meal Extract, Sebacic Acid, Sodium Polyacrylate, Propylene Glycol, Fragrance (Parfum), Benzyl Alcohol, Linalool, Hydroxycitronellal, Alpha-Isomethyl Ionone, Amyl Cinnamal, Hexyl Cinnamal, Evernia Furfuracea (Treemoss) Extract, Geraniol, Benzyl Benzoate, Butylphenyl Methylpropional, Methylparaben, Ethylparaben, Butylparaben, Potassium Sorbate

image of cartonimage of carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

La Prairie Switzerland

Cellular Blemish Control

15 ml / 0.5 FL.OZ.

image of primary labelimage of primary label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59614-311-022019-10-21C16284748780-1956f9ecf-d2a2-621f-e053-dbdaa90a74adCellular Blemish Control

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59614-311-01La Prairie Switzerland Cellular Blemish Control15 mL in 1 BOTTLECREAM151
59614-311-02La Prairie Switzerland Cellular Blemish Control1 in 1 BOXCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59614-311LA PRAIRIE SWITZERLAND (SALICYLIC ACID) CREAM [JUVENA PRODUITS DE BEAUTE GMBH]1Legacy NDC, 2 package rows20100602_ed12e2ef-dd57-4026-8f1b-40daf560901e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SALICYLIC ACIDACTIVE INGREDIENTO414PZ4LPZ1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59614-31159614-311-01, 59614-311-02

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB

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
148adfb5-b153-4f3f-b5bc-b040c2f8e63bed12e2ef-dd57-4026-8f1b-40daf560901e2010-06-02WarningsExact identifier
spl id: 148adfb5-b153-4f3f-b5bc-b040c2f8e63b
spl set id: ed12e2ef-dd57-4026-8f1b-40daf560901e

Reported adverse events (FAERS/openFDA)#

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