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  4. NDC Product Code: 11559-729 Double Wear Stay In Place Spf 10 Makeup

NDC 11559-729 Double Wear Stay In Place Spf 10 Makeup

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11559-729?
  4. Double Wear Stay In Place Spf 10 Makeup Uses
  5. Active Ingredients UNII Codes
  6. 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:
11559-729
Proprietary Name:
Double Wear Stay In Place Spf 10 Makeup
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Estee Lauder Inc
Labeler Code:
11559
Product Label ID:
33587c55-12a6-4312-bb1c-034d43835837
FDA Application Number: [6]
part352
Marketing Category: [8]
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date: [9]
03-01-2007
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 11559-729?

The NDC code 11559-729 is assigned by the FDA to the product Double Wear Stay In Place Spf 10 Makeup 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 11559-729-01 1 jar in 1 carton / 12 g in 1 jar (11559-729-02). 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.

What are the uses for Double Wear Stay In Place Spf 10 Makeup?

INACTIVE INGREDIENTS: TALC [] ISOSTEARYL PALMITATE [] SILICA [] CALCIUM SILICATE [] BORON NITRIDE [] METHICONE [] TRIMETHYLSILOXYSILICATE [] PHENYL TRIMETHICONE [] POLYMETHYLSILSESQUIOXANE [] METHYL METHACRYLATE CROSSPOLYMER [] CAPRYLYL GLYCOL [] ADIPIC ACID/NEOPENTYL GLYCOL CROSSPOLYMER [] POLYPROPYLENE [] HEXYLENE GLYCOL [] PHENOXYETHANOL []  [+/- IRON OXIDES (CI 77491, CI 77492, CI 77499) [] MICA [] CHROMIUM OXIDE GREENS (CI 77288) [] CHROMIUM HYDROXIDE GREEN (CI 77289) [] CARMINE (CI 75470) [] BISMUTH OXYCHLORIDE (CI 77163) [] TITANIUM DIOXIDE (CI 77891)]

Which are Double Wear Stay In Place Spf 10 Makeup UNII Codes?

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

Which are Double Wear Stay In Place Spf 10 Makeup 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:

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Product Footnotes

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

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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".