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NDC 69153-120 An Tooth

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69153-120?
  4. An Tooth Uses
  5. Active Ingredients UNII Codes
  6. 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:
69153-120
Proprietary Name:
An Tooth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
An Co Ltd.
Labeler Code:
69153
Product Label ID:
0989102a-cf0c-4ddb-9f0e-5b2c85c93ddd
Start Marketing Date: [9]
02-01-2017
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69153-120-02

Package Description: 1 TUBE in 1 CARTON / 160 g in 1 TUBE (69153-120-01)

Product Details

What is NDC 69153-120?

The NDC code 69153-120 is assigned by the FDA to the product An Tooth which is product labeled by An Co Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69153-120-02 1 tube in 1 carton / 160 g in 1 tube (69153-120-01). 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 An Tooth?

Directions: Brush teeth with balance of toothpaste. Directions: Brush teeth with balance of toothpaste.

Which are An Tooth UNII Codes?

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

Which are An Tooth 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:

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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".