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  4. NDC Product Code: 79481-0500 Soft Tip Neti Pot Sinus Wash Meijer

NDC 79481-0500 Soft Tip Neti Pot Sinus Wash Meijer

Sodium Bicarbonate,Sodium Chloride Kit Nasal - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 79481-0500?
  4. Soft Tip Neti Pot Sinus Wash Meijer Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
79481-0500
Proprietary Name:
Soft Tip Neti Pot Sinus Wash Meijer
Non-Proprietary Name: [1]
Sodium Bicarbonate, Sodium Chloride
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Administration Route(s): [4]
  • Nasal - Administration to the nose; administered by way of the nose.
    • Labeler Name: [5]
    Meijer, Inc.
    Labeler Code:
    79481
    Product Label ID:
    dd7437b7-5224-aaed-e053-2995a90a1b65
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    01-09-2022
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 79481-0500-1

    Package Description: 1 KIT in 1 KIT * 3000 mg in 1 PACKET (42829-998-00)

    Product Details

    What is NDC 79481-0500?

    The NDC code 79481-0500 is assigned by the FDA to the product Soft Tip Neti Pot Sinus Wash Meijer which is a human over the counter drug product labeled by Meijer, Inc.. The generic name of Soft Tip Neti Pot Sinus Wash Meijer is sodium bicarbonate, sodium chloride. The product's dosage form is kit and is administered via nasal form. The product is distributed in a single package with assigned NDC code 79481-0500-1 1 kit in 1 kit * 3000 mg in 1 packet (42829-998-00). 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 Soft Tip Neti Pot Sinus Wash Meijer?

    UsesTemporarily relieves symptoms associated withsinusitis, cold, flu or allergies-Sneezing-Nasal Stuffiness-Runny nose-Post nasal dripRemoves inhaled irritants (dust, pollen)Removes nasal and sinus drainageHelps reduce swelling of nasal membranesMoisturizes dry nasal passages

    Which are Soft Tip Neti Pot Sinus Wash Meijer UNII Codes?

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

    Which are Soft Tip Neti Pot Sinus Wash Meijer 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 Soft Tip Neti Pot Sinus Wash Meijer?

    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: 1542919 - sodium bicarbonate 700 MG / sodium chloride 2300 MG Powder for Nasal Solution
    • RxCUI: 1542919 - NaHCO3 700 MG / NaCl 2300 MG Powder for Nasal Solution

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [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".