1. Labeler Index
  2. Clinique Laboratories Inc
  3. NDC Product Code: 49527-707 Super Defense Superdefense Age Defense Moisturizer Spf 25 Dry Combination

NDC 49527-707 Super Defense Superdefense Age Defense Moisturizer Spf 25 Dry Combination

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 49527-707?
    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:
49527-707
Proprietary Name:
Super Defense Superdefense Age Defense Moisturizer Spf 25 Dry Combination
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Clinique Laboratories Inc
Labeler Code:
49527
Product Label ID:
02e18eef-3ef1-4f02-a031-c127d0836f31
Start Marketing Date: [9]
04-01-2008
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 49527-707-01

Package Description: 1 JAR in 1 CARTON / 50 mL in 1 JAR (49527-707-02)

Product Details

What is NDC 49527-707?

The NDC code 49527-707 is assigned by the FDA to the product Super Defense Superdefense Age Defense Moisturizer Spf 25 Dry Combination which is product labeled by Clinique Laboratories Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49527-707-01 1 jar in 1 carton / 50 ml in 1 jar (49527-707-02). 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 Super Defense Superdefense Age Defense Moisturizer Spf 25 Dry Combination UNII Codes?

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

Which are Super Defense Superdefense Age Defense Moisturizer Spf 25 Dry Combination 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.

[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".