1. Home
  2. Labeler Index
  3. Estee Lauder Inc
  4. NDC Product Code: 11559-737 Time Zone Line And Wrinkle Reducing Creme Spf 15 Normal Combo Skin

NDC 11559-737 Time Zone Line And Wrinkle Reducing Creme Spf 15 Normal Combo Skin

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11559-737?
  4. Active Ingredients UNII Codes
  5. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11559-737
Proprietary Name:
Time Zone Line And Wrinkle Reducing Creme Spf 15 Normal Combo Skin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Estee Lauder Inc
Labeler Code:
11559
Product Label ID:
4f6a335a-c6df-4076-b6b5-371ecb03be29
Start Marketing Date: [9]
11-01-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11559-737-01

Package Description: 1 JAR in 1 CARTON / 50 mL in 1 JAR (11559-737-02)

Product Details

What is NDC 11559-737?

The NDC code 11559-737 is assigned by the FDA to the product Time Zone Line And Wrinkle Reducing Creme Spf 15 Normal Combo Skin which is product labeled by Estee Lauder Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11559-737-01 1 jar in 1 carton / 50 ml in 1 jar (11559-737-02). 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.

Which are Time Zone Line And Wrinkle Reducing Creme Spf 15 Normal Combo Skin UNII Codes?

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

Which are Time Zone Line And Wrinkle Reducing Creme Spf 15 Normal Combo Skin Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive 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".