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  4. NDC Product Code: 73430-0007 Dr.nuell Vanishing Bb

NDC 73430-0007 Dr.nuell Vanishing Bb

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73430-0007?
  4. Dr.nuell Vanishing Bb 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:
73430-0007
Proprietary Name:
Dr.nuell Vanishing Bb
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Apharm Co., Ltd.
Labeler Code:
73430
Product Label ID:
970b09b1-7808-435c-e053-2a95a90a9b3c
Start Marketing Date: [9]
11-01-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73430-0007-1

Package Description: 30 mL in 1 TUBE

Product Details

What is NDC 73430-0007?

The NDC code 73430-0007 is assigned by the FDA to the product Dr.nuell Vanishing Bb which is product labeled by Apharm Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73430-0007-1 30 ml 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 Dr.nuell Vanishing Bb?

Use BB cream alone, or take the appropriate amount and apply it evenly along with the skin texture in the last stage of skin care

Which are Dr.nuell Vanishing Bb UNII Codes?

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

Which are Dr.nuell Vanishing Bb 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".