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  4. NDC Product Code: 49963-381 Brontuss Sf-nr

NDC 49963-381 Brontuss Sf-nr

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 49963-381?
  5. Brontuss Sf-nr 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:
49963-381
Proprietary Name:
Brontuss Sf-nr
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Portal Pharmaceutical
Labeler Code:
49963
Product Label ID:
5732c79c-9717-498b-b511-f6da2dfbb867
Start Marketing Date: [9]
12-22-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)

Code Structure Chart

Product Details

What is NDC 49963-381?

The NDC code 49963-381 is assigned by the FDA to the product Brontuss Sf-nr which is product labeled by Portal Pharmaceutical. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 49963-381-01 30 ml in 1 bottle , 49963-381-04 118 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 Brontuss Sf-nr?

Do not exceed recommended dosage.Adults and Children 12years of ageand over:1 teaspoonful (5 mL)every 4 hours, not toexceed 6 doses in 24hours.Children 6 tounder 12years of age:1/2 teaspoonful (2.5 mL)every 4 hours, not toexceed 6 doses in 24hours.Children under 6 yearsof age:Consult a doctor.

Which are Brontuss Sf-nr UNII Codes?

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

Which are Brontuss Sf-nr 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 Brontuss Sf-nr?

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: 1251031 - dextromethorphan HBr 15 MG / guaiFENesin 300 MG / phenylephrine HCl 10 MG in 5 mL Oral Solution
  • RxCUI: 1251031 - dextromethorphan hydrobromide 3 MG/ML / guaifenesin 60 MG/ML / phenylephrine hydrochloride 2 MG/ML Oral Solution
  • RxCUI: 1251031 - dextromethorphan HBr 15 MG / guaifenesin 300 MG / phenylephrine HCl 10 MG per 5 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".