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NDC 0363-0540 Hydrating Antioxidant Moiturizer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0363-0540?
  4. Hydrating Antioxidant Moiturizer 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:
0363-0540
Proprietary Name:
Hydrating Antioxidant Moiturizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Company
Labeler Code:
0363
Product Label ID:
dbf44ea9-1073-4a8f-b44b-2bf1a1b48081
Start Marketing Date: [9]
10-28-2017
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0363-0540-01

Package Description: 118 mL in 1 PACKAGE

Product Details

What is NDC 0363-0540?

The NDC code 0363-0540 is assigned by the FDA to the product Hydrating Antioxidant Moiturizer which is product labeled by Walgreen Company. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-0540-01 118 ml in 1 package . 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 Hydrating Antioxidant Moiturizer?

Uses  •helps prevent sunburn  •If used as directedwith other protection measures (seeDirections), decreases the risk of skin cancer andearly skin aging caused by the sun.

Which are Hydrating Antioxidant Moiturizer UNII Codes?

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

Which are Hydrating Antioxidant Moiturizer 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".