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  4. NDC Product Code: 69255-200 Dr. 9020 Dental Clinic

NDC 69255-200 Dr. 9020 Dental Clinic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69255-200?
  4. Dr. 9020 Dental Clinic 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:
69255-200
Proprietary Name:
Dr. 9020 Dental Clinic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jangin Pharm Co.,ltd.
Labeler Code:
69255
Product Label ID:
7f10d5a6-2d5b-7ce2-e053-2991aa0ab425
Start Marketing Date: [9]
09-01-2018
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69255-200-01

Package Description: 260 mL in 1 BOTTLE

Product Details

What is NDC 69255-200?

The NDC code 69255-200 is assigned by the FDA to the product Dr. 9020 Dental Clinic which is product labeled by Jangin Pharm Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69255-200-01 260 ml in 1 bottle . 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 Dr. 9020 Dental Clinic?

● Administration and doses : Once a day (mainly before bed), use it after brushing thoroughly. 6 years old to adults:10ml into your mouth, mix well for 1 minute, then spit. Be careful not to eat or drink food for 30 minutes after use to obtain sufficient effect.

Which are Dr. 9020 Dental Clinic UNII Codes?

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

Which are Dr. 9020 Dental Clinic 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".