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  4. NDC Product Code: 0363-1103 Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit

NDC 0363-1103 Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0363-1103?
  5. Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
0363-1103
Proprietary Name:
Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Co.
Labeler Code:
0363
Product Label ID:
1f336dce-df94-4c93-b901-17efc0b899d7
Start Marketing Date: [9]
06-11-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - CARAMEL COLOR)
YELLOW (C48330 - D AND C YELLOW 10)
YELLOW (C48330 - D AND C YELLOW NO. 10)
Flavor(s):
HONEY (C73394 - NATURAL HONEY AND LEMON FLAVOR)
LEMON (C73396 - NATURAL HONEY AND LEMON FLAVOR)

Code Structure Chart

Product Details

What is NDC 0363-1103?

The NDC code 0363-1103 is assigned by the FDA to the product Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit which is product labeled by Walgreen Co.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-1103-12 1 kit in 1 box * 6 granule, for solution in 1 box * 6 granule, for solution in 1 box. 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 Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit?

When using this product- do not exceed recommended dosage - avoid alcoholic drinks - marked drowsiness may occur - alcohol, sedatives and tranquilizers may increase drowsiness - be careful when driving a motor vehicle or operating machinery - excitability may occur, especially in children. When using this product - do not exceed recommended dosage.

Which are Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit UNII Codes?

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

Which are Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit 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 Well At Walgreens Multi-symptom Wal-flu Severe Cold And Nighttime Wal-flu Severe Cold And Cough Kit?

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: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Packet for Oral Solution
  • RxCUI: 1189316 - acetaminophen 500 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Powder for Oral Solution
  • RxCUI: 1189316 - APAP 500 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for Oral Solution

* 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".