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  4. NDC Product Code: 11673-408 Saline Wash

NDC 11673-408 Saline Wash

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11673-408?
  4. Saline Wash Uses
  5. Active 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:
11673-408
Proprietary Name:
Saline Wash
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Target Corporation
Labeler Code:
11673
Product Label ID:
e3fc498d-2bdc-4464-b893-58e8663b067b
Start Marketing Date: [9]
04-01-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11673-408-00

Package Description: 100 PACKET in 1 CARTON / 1 POWDER, FOR SOLUTION in 1 PACKET

Product Details

What is NDC 11673-408?

The NDC code 11673-408 is assigned by the FDA to the product Saline Wash which is product labeled by Target Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11673-408-00 100 packet in 1 carton / 1 powder, for solution in 1 packet. 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 Saline Wash?

UsesTemporarily relieves symptoms associated with sinusitis, colds, flu or allergiesSneezingRunny noseNasal stuffinessPost nasal dripRemoves inhaled irritants (dust, pollen)Promotes nasal and sinus drainageHelps reduce swelling of nasal membranes

Which are Saline Wash UNII Codes?

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

* 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".