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NDC 59779-063 Cvs Advanced Deep Set Wrinkle Therapy W/spf15

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59779-063?
  4. Cvs Advanced Deep Set Wrinkle Therapy W/spf15 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:
59779-063
Proprietary Name:
Cvs Advanced Deep Set Wrinkle Therapy W/spf15
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy
Labeler Code:
59779
Product Label ID:
190c28dd-4b9a-4410-a48d-bfff81fa21a5
Start Marketing Date: [9]
07-19-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 59779-063?

The NDC code 59779-063 is assigned by the FDA to the product Cvs Advanced Deep Set Wrinkle Therapy W/spf15 which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-063-09 50 ml in 1 bottle, pump . 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 Cvs Advanced Deep Set Wrinkle Therapy W/spf15?

Recomended regimenStep 1 Cleanse skin thoroughlyStep 2 Apply CVS/pharmacy Day and Night Eye CreamStep 3 AM: Follow-up with CVS/pharmacy Deep-Set Wrinkle Day Treatment.           PM: CVS/pharmacy Deep-Set Wrinkle Night Cream.How and When to UseEvery morning after thoroughly cleansing skin, apply alone or under makeup. Gently smooth onto face and neck until completely absorbed.To use as a sunscreen apply to face prior to sun exposure

Which are Cvs Advanced Deep Set Wrinkle Therapy W/spf15 UNII Codes?

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

Which are Cvs Advanced Deep Set Wrinkle Therapy W/spf15 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".