1. Home
  2. Labeler Index
  3. Natural Korea Co., Ltd.
  4. NDC Product Code: 74646-0016 Dabida Extreme Skin Tag Remover

NDC 74646-0016 Dabida Extreme Skin Tag Remover

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 74646-0016?
  4. Active Ingredients UNII Codes
  5. 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:
74646-0016
Proprietary Name:
Dabida Extreme Skin Tag Remover
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Natural Korea Co., Ltd.
Labeler Code:
74646
Product Label ID:
b2a18fac-6b74-2ff4-e053-2995a90aff7b
Start Marketing Date: [9]
10-27-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 74646-0016-1

Package Description: 1 TUBE, WITH APPLICATOR in 1 BOX / 15 mL in 1 TUBE, WITH APPLICATOR

Product Details

What is NDC 74646-0016?

The NDC code 74646-0016 is assigned by the FDA to the product Dabida Extreme Skin Tag Remover which is product labeled by Natural Korea Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 74646-0016-1 1 tube, with applicator in 1 box / 15 ml in 1 tube, 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.

Which are Dabida Extreme Skin Tag Remover UNII Codes?

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

  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)

Which are Dabida Extreme Skin Tag Remover 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".