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NDC 0363-7779 Antiseptic Pain Relieving

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 0363-7779?
  4. Active Ingredients UNII Codes
  5. Inactive Ingredients UNII Codes
  6. 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:
0363-7779
Proprietary Name:
Antiseptic Pain Relieving
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreens
Labeler Code:
0363
Product Label ID:
3c418897-e559-4bff-a1e4-ee1ca76269f8
Start Marketing Date: [9]
07-31-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 0363-7779-03

Package Description: 85 g in 1 CAN

Product Details

What is NDC 0363-7779?

The NDC code 0363-7779 is assigned by the FDA to the product Antiseptic Pain Relieving which is product labeled by Walgreens. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-7779-03 85 g in 1 can . 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 Antiseptic Pain Relieving UNII Codes?

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

Which are Antiseptic Pain Relieving 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 Antiseptic Pain Relieving?

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:
  • RxCUI: 2043455 - benzalkonium chloride 0.1 % / benzocaine 20 % Topical Spray
  • RxCUI: 2043455 - benzalkonium chloride 1 MG/ML / benzocaine 200 MG/ML Topical Spray
  • RxCUI: 2043455 - benzalkonium Cl 0.1 % / benzocaine 20 % Topical Spray

* Please review the disclaimer below.

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".