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NDC 59779-749 Beauty 360 Daily Moisturizing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59779-749?
  4. Beauty 360 Daily Moisturizing Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59779-749
Proprietary Name:
Beauty 360 Daily Moisturizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy
Labeler Code:
59779
Product Label ID:
3143f652-fc8d-4506-a035-ba5dedbcd0b3
Start Marketing Date: [9]
02-02-2017
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 59779-749?

The NDC code 59779-749 is assigned by the FDA to the product Beauty 360 Daily Moisturizing which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 59779-749-02 71 ml in 1 tube , 59779-749-08 227 ml in 1 tube , 59779-749-12 355 ml in 1 bottle, plastic , 59779-749-18 532 ml in 1 bottle, plastic . 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 Beauty 360 Daily Moisturizing?

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Which are Beauty 360 Daily Moisturizing UNII Codes?

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

Which are Beauty 360 Daily Moisturizing 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:

What is the NDC to RxNorm Crosswalk for Beauty 360 Daily Moisturizing?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".