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  4. NDC Product Code: 15187-004 Scot-tussin Original Multi-symptom Cold And Allergy Relief

NDC 15187-004 Scot-tussin Original Multi-symptom Cold And Allergy Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 15187-004?
  5. Scot-tussin Original Multi-symptom Cold And Allergy 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:
15187-004
Proprietary Name:
Scot-tussin Original Multi-symptom Cold And Allergy Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Irisys, Llc
Labeler Code:
15187
Product Label ID:
ce11862b-24c6-4d51-87a9-930858a47de5
Start Marketing Date: [9]
01-01-2016
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - CLEAR CHERRY-STRAWBERRY FLAVOR)
STRAWBERRY (C73417 - CLEAR CHERRY-STRAWBERRY FLAVOR)

Product Packages

NDC Code 15187-004-04

Package Description: 1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE

Product Details

What is NDC 15187-004?

The NDC code 15187-004 is assigned by the FDA to the product Scot-tussin Original Multi-symptom Cold And Allergy Relief which is product labeled by Irisys, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 15187-004-04 1 bottle in 1 carton / 118 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 Scot-tussin Original Multi-symptom Cold And Allergy Relief?

Do not use more than directed – see Liver warning.follow Dosage Chart.do not take more than 4 doses in any 24 hour period.this product is not intended for use in children under 12 years of age.       agedoseAdults and children over 12 years old2 teaspoons (2 tsp. 10 mL) every 6 hoursChildren under 12 years oldDO NOT USE

Which are Scot-tussin Original Multi-symptom Cold And Allergy Relief UNII Codes?

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

Which are Scot-tussin Original Multi-symptom Cold And Allergy 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 Scot-tussin Original Multi-symptom Cold And Allergy 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: 1367384 - acetaminophen 160 MG / pheniramine maleate 4 MG / phenylephrine HCl 4 MG in 5 mL Oral Solution
  • RxCUI: 1367384 - acetaminophen 32 MG/ML / pheniramine maleate 0.8 MG/ML / phenylephrine hydrochloride 0.8 MG/ML Oral Solution
  • RxCUI: 1367384 - acetaminophen 160 MG / pheniramine maleate 4 MG / phenylephrine HCl 4 MG per 5 ML Oral Solution
  • RxCUI: 1367384 - APAP 32 MG/ML / Pheniramine Maleate 0.8 MG/ML / Phenylephrine Hydrochloride 0.8 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".