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  4. NDC Product Code: 0363-1005 Nighttime Cold And Flu Relief

NDC 0363-1005 Nighttime Cold And Flu Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0363-1005?
  5. Nighttime Cold And Flu Relief 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:
0363-1005
Proprietary Name:
Nighttime Cold And Flu Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreen Company
Labeler Code:
0363
Product Label ID:
6461e6af-6cb3-7fcd-477c-838fe816cf4f
Start Marketing Date: [9]
10-09-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
OVAL (C48345)
Size(s):
20 MM
Imprint(s):
35A
Score:
1

Code Structure Chart

Product Details

What is NDC 0363-1005?

The NDC code 0363-1005 is assigned by the FDA to the product Nighttime Cold And Flu Relief which is product labeled by Walgreen Company. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 0363-1005-01 2 blister pack in 1 carton / 8 capsule, liquid filled in 1 blister pack, 0363-1005-02 2 blister pack in 1 carton / 12 capsule, liquid filled in 1 blister pack. 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 Nighttime Cold And Flu Relief?

Do not take more than directed (see overdose warning)do not take more than 8 liquid caps in 24 hoursadults and children 12 years and over: take 2 liquid caps with water every 6 hourschildren under 12 years: do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause   liver damage.

Which are Nighttime Cold And Flu Relief UNII Codes?

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

Which are Nighttime Cold And Flu Relief 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 Nighttime Cold And Flu Relief?

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: 1094549 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule
  • RxCUI: 1094549 - APAP 325 MG / dextromethorphan hydrobromide 15 MG / doxylamine succinate 6.25 MG Oral Capsule

* 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".