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  4. NDC Product Code: 53304-0306 Eb306 Nasal Decongestant

NDC 53304-0306 Eb306 Nasal Decongestant

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53304-0306?
  4. Eb306 Nasal Decongestant Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
53304-0306
Proprietary Name:
Eb306 Nasal Decongestant
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Eminence Biotech Corporation Limited
Labeler Code:
53304
Product Label ID:
887562bf-1b9d-4980-8859-5d8d8a723994
Start Marketing Date: [9]
11-01-2012
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53304-0306-1

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 15 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 53304-0306?

The NDC code 53304-0306 is assigned by the FDA to the product Eb306 Nasal Decongestant which is product labeled by Eminence Biotech Corporation Limited. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53304-0306-1 1 bottle, spray in 1 box / 15 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 Eb306 Nasal Decongestant?

This product is used as Nasal Decongestant. For the temporary relief of nasal congestion due to hay fever or other upper respiratory allergies (allergic rhinitis)

Which are Eb306 Nasal Decongestant UNII Codes?

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

Which are Eb306 Nasal Decongestant 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 Eb306 Nasal Decongestant?

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:

* Please review the disclaimer below.

Patient Education

Phenylephrine Nasal Spray


Phenylephrine nasal spray is used to relieve nasal discomfort caused by colds, allergies, and hay fever. It is also used to relieve sinus congestion and pressure. Phenylephrine nasal spray will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Phenylephrine is in a class of medications called nasal decongestants. It works by reducing swelling of the blood vessels in the nasal passages.
[Learn More]


* 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".