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  4. NDC Product Code: 72191-0100 Adea Gargle

NDC 72191-0100 Adea Gargle

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72191-0100?
  5. Adea Gargle Uses
  6. Active Ingredients UNII Codes
  7. 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:
72191-0100
Proprietary Name:
Adea Gargle
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
K2resource Co., Ltd.
Labeler Code:
72191
Product Label ID:
684a39f7-434d-532f-e053-2a91aa0a4f8b
Start Marketing Date: [9]
03-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
BULLET (C48335)
Size(s):
17 MM
Imprint(s):
NONE
Flavor(s):
PEPPERMINT (C73408)

Code Structure Chart

Product Details

What is NDC 72191-0100?

The NDC code 72191-0100 is assigned by the FDA to the product Adea Gargle which is product labeled by K2resource Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72191-0100-1 850 mg in 1 bottle, plastic . 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 Adea Gargle?

Put a tablet of Adea Gargle in your mouth and chew or melt according to your preference.When foaming starts, please gaggle for more than 30 seconds so that every corner of the mouth can reach Adea Gaggle.When the gaggle is over, spit or swallow the bubbles.

Which are Adea Gargle UNII Codes?

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

Which are Adea Gargle 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:

* 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".