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  4. NDC Product Code: 52904-456 Cold Relief Severe Pain Cough

NDC 52904-456 Cold Relief Severe Pain Cough

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52904-456?
  5. Cold Relief Severe Pain Cough 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:
52904-456
Proprietary Name:
Cold Relief Severe Pain Cough
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Select Corporation
Labeler Code:
52904
Product Label ID:
f38a784b-cfc3-4238-9cd3-56c1dba94e6f
Start Marketing Date: [9]
10-15-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - SNOW WHITE)
Shape:
ROUND (C48348)
Size(s):
12 MM
Imprint(s):
FR12
Score:
1

Product Packages

NDC Code 52904-456-02

Package Description: 2 TABLET in 1 PACKET

Product Details

What is NDC 52904-456?

The NDC code 52904-456 is assigned by the FDA to the product Cold Relief Severe Pain Cough which is product labeled by Select Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52904-456-02 2 tablet in 1 packet . 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 Cold Relief Severe Pain Cough?

Uses: or the temporary relief of the following cold symptoms: • minor aches and pains • headache • sore throat • nasal congestion • cough • helps loose phlegm (mucus) and thin bronchial secretions to make coughs more  productive • temporarily reduces fever

Which are Cold Relief Severe Pain Cough UNII Codes?

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

Which are Cold Relief Severe Pain Cough 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 Cold Relief Severe Pain Cough?

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: 1294471 - acetaminophen 325 MG / dextromethorphan HBr 15 MG / guaiFENesin 200 MG / pseudoephedrine HCl 30 MG Oral Tablet
  • RxCUI: 1294471 - acetaminophen 325 MG / dextromethorphan hydrobromide 15 MG / guaifenesin 200 MG / pseudoephedrine hydrochloride 30 MG Oral Tablet
  • RxCUI: 1294471 - APAP 325 MG / Dextromethorphan Hydrobromide 15 MG / Guaifenesin 200 MG / Pseudoephedrine Hydrochloride 30 MG Oral Tablet

* 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".