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  4. NDC Product Code: 61715-074 Cough Multi Symptom

NDC 61715-074 Cough Multi Symptom

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61715-074?
  5. Cough Multi Symptom 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:
61715-074
Proprietary Name:
Cough Multi Symptom
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kinray Llc
Labeler Code:
61715
Product Label ID:
08dadb5c-38e2-41e2-9963-83f98025330a
Start Marketing Date: [9]
08-28-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - CLEAR)
Flavor(s):
MENTHOL (C73403)

Code Structure Chart

Product Details

What is NDC 61715-074?

The NDC code 61715-074 is assigned by the FDA to the product Cough Multi Symptom which is product labeled by Kinray Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61715-074-08 236 ml in 1 bottle . 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 Cough Multi Symptom?

Take only as recommended - see overdose warninguse dose cup or Tabelspoon (TBSP)do not take more than 10 tablespoons (tbsp) or 150 mL in 24-hours periodAdults and children 12 years of ageand overtake 2 tablespoons (tbsp) 30 ml in dose cup provided every 6 hours as needed Children under 12 yearsdo not use this product in children under 12 years of age: this will provide more than the recommended dose (overdose) and may cause liver damage

Which are Cough Multi Symptom UNII Codes?

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

Which are Cough Multi Symptom 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 Cough Multi Symptom?

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: 1242502 - acetaminophen 500 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG in 15 mL Oral Solution
  • RxCUI: 1242502 - acetaminophen 33.3 MG/ML / dextromethorphan hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML / phenylephrine hydrochloride 0.333 MG/ML Oral Solution
  • RxCUI: 1242502 - acetaminophen 500 MG / dextromethorphan HBr 15 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG per 15 ML Oral Solution
  • RxCUI: 1242502 - APAP 33.3 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML / doxylamine succinate 0.417 MG/ML / Phenylephrine Hydrochloride 0.333 MG/ML 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".