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  4. NDC Product Code: 50441-0002 Allergy And Hay Fever

NDC 50441-0002 Allergy And Hay Fever

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50441-0002?
  4. Allergy And Hay Fever Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
50441-0002
Proprietary Name:
Allergy And Hay Fever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pharmwest Inc.
Labeler Code:
50441
Product Label ID:
daa55ea7-491d-4321-bd02-8118e4fb744d
Start Marketing Date: [9]
11-08-2012
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 50441-0002?

The NDC code 50441-0002 is assigned by the FDA to the product Allergy And Hay Fever which is product labeled by Pharmwest Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50441-0002-2 59 ml in 1 bottle, spray . 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 Allergy And Hay Fever?

Uses: For the temporary relief of allergy and hay fever symptoms due to seasonal allergies, rhinitus, sinus congestion and pain, itchy, red and watery eyes, sneezing, runny nose, postnasal drip, cough and sore throat. Will not cause drowsiness.

Which are Allergy And Hay Fever UNII Codes?

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

Which are Allergy And Hay Fever 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:

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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".