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  4. NDC Product Code: 73065-0004 Hae Yan Tooth

NDC 73065-0004 Hae Yan Tooth

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73065-0004?
  4. Hae Yan 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:
73065-0004
Proprietary Name:
Hae Yan Tooth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Woorilife&health
Labeler Code:
73065
Product Label ID:
a6c5d725-0972-642f-e053-2995a90a0126
Start Marketing Date: [9]
05-25-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 73065-0004?

The NDC code 73065-0004 is assigned by the FDA to the product Hae Yan Tooth which is product labeled by Woorilife&health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73065-0004-1 130 g in 1 tube . 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 Hae Yan Tooth?

Adults and children 2 years of age and olderBrush teeth thoroughly preferably after each meal or at least twice a day or as directed by a dentist or docter.Children under 6 yearsTo minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.Children under 2 years Consult a dentist or doctor

Which are Hae Yan Tooth UNII Codes?

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

Which are Hae Yan 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".