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  4. NDC Product Code: 42469-2001 Stomint

NDC 42469-2001 Stomint

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 42469-2001?
  5. Stomint 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:
42469-2001
Proprietary Name:
Stomint
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Evercarepharm Co., Ltd
Labeler Code:
42469
Product Label ID:
0ddae254-1ead-40d3-a56e-155ae121761a
Start Marketing Date: [9]
06-06-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
OVAL (C48345)
Size(s):
20 MM
Imprint(s):
3;HP;X
Score:
1

Product Packages

NDC Code 42469-2001-1

Package Description: 90 TABLET in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 42469-2001?

The NDC code 42469-2001 is assigned by the FDA to the product Stomint which is product labeled by Evercarepharm Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 42469-2001-1 90 tablet in 1 bottle, with applicator . 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 Stomint?

Take 3 times a day after meals with warm water

Which are Stomint UNII Codes?

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

  • ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)
  • ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O) (Active Moiety)

Which are Stomint 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".