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  4. NDC Product Code: 63824-161 Delsym Cough Relief Plus Soothing Action

NDC 63824-161 Delsym Cough Relief Plus Soothing Action

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63824-161?
  5. Delsym Cough Relief Plus Soothing Action 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:
63824-161
Proprietary Name:
Delsym Cough Relief Plus Soothing Action
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reckitt Benckiser Llc
Labeler Code:
63824
Product Label ID:
bc0334df-0f75-4be9-b922-f3e0fc7289a6
Start Marketing Date: [9]
07-01-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
ROUND (C48348)
Size(s):
27 MM
Imprint(s):
D
Score:
1
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 63824-161?

The NDC code 63824-161 is assigned by the FDA to the product Delsym Cough Relief Plus Soothing Action which is product labeled by Reckitt Benckiser Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63824-161-16 16 lozenge 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 Delsym Cough Relief Plus Soothing Action?

This medication is used for temporary relief of coughs without phlegm that are caused by certain infections of the air passages (e.g., sinusitis, common cold). This product should not usually be used for an ongoing cough from smoking or long-term breathing problems (e.g., chronic bronchitis, emphysema) unless directed by your doctor. This product contains dextromethorphan. It is a cough suppressant that works by decreasing the feeling of needing to cough. Cough-and-cold products have not been shown to be safe or effective in children younger than 6 years. Therefore, do not use this product to treat cold symptoms in children younger than 6 years unless specifically directed by the doctor. Ask your doctor or pharmacist for more details about using your product safely. These products do not cure or shorten the length of the common cold and may cause serious side effects. To decrease the risk for serious side effects, carefully follow all dosage directions. Do not use this product to make a child sleepy. Do not give other cough-and-cold medication that might contain the same or similar ingredients (see also Drug Interactions section). Ask the doctor or pharmacist about other ways to relieve cough and cold symptoms (such as drinking enough fluids, using a humidifier or saline nose drops/spray).

Which are Delsym Cough Relief Plus Soothing Action UNII Codes?

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

Which are Delsym Cough Relief Plus Soothing Action 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 Delsym Cough Relief Plus Soothing Action?

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: 1301246 - dextromethorphan HBr 5 MG / menthol 5 MG Oral Lozenge
  • RxCUI: 1301246 - dextromethorphan hydrobromide 5 MG / menthol 5 MG Oral Lozenge

* 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".