NDC 37205-752 Kettle Neti Pot

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
37205-752
Proprietary Name:
Kettle Neti Pot
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health 414, Llc
Labeler Code:
37205
Start Marketing Date: [9]
04-01-2013
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 37205-752-03

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

Product Details

What is NDC 37205-752?

The NDC code 37205-752 is assigned by the FDA to the product Kettle Neti Pot which is product labeled by Cardinal Health 414, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37205-752-03 100 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 Kettle Neti Pot?

UsesTemporarily relieves symptoms associated with sinusitis, cold, flu or allergies:-Sneezing-Nasal Stuffiness-Runny Nose-Post nasal dripRemoves inhaled irritants (dust, pollen)Promotes nasal and sinus drainageHelps reduce swelling of nasal membranes

Which are Kettle Neti Pot 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".