NDC 59614-301 La Prairie Switzerland Cellular Radiance Emulsion

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59614-301
Proprietary Name:
La Prairie Switzerland Cellular Radiance Emulsion
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Juvena Produits De Beaute
Labeler Code:
59614
Start Marketing Date: [9]
01-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59614-301-02

Package Description: 1 TUBE in 1 BOX / 50 mL in 1 TUBE (59614-301-01)

Product Details

What is NDC 59614-301?

The NDC code 59614-301 is assigned by the FDA to the product La Prairie Switzerland Cellular Radiance Emulsion which is product labeled by Juvena Produits De Beaute. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59614-301-02 1 tube in 1 box / 50 ml in 1 tube (59614-301-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for La Prairie Switzerland Cellular Radiance Emulsion?

Uses-helps prevent sunburn-for skin that burns easily-provides moderate protection against sunburn-higher SPF gives more sunburn protectionDirections-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

Which are La Prairie Switzerland Cellular Radiance Emulsion UNII Codes?

The UNII codes for the active ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".