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  4. NDC Product Code: 70929-0002 Antibe Beausenne Special Ampoule

NDC 70929-0002 Antibe Beausenne Special Ampoule

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70929-0002?
  4. Antibe Beausenne Special Ampoule 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:
70929-0002
Proprietary Name:
Antibe Beausenne Special Ampoule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Modongee Co., Ltd.
Labeler Code:
70929
Product Label ID:
f9505acc-a44f-432b-8bdd-cb15447c672f
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70929-0002?

The NDC code 70929-0002 is assigned by the FDA to the product Antibe Beausenne Special Ampoule which is product labeled by Modongee Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70929-0002-2 4 bottle, dropper in 1 box / 50 ml in 1 bottle, dropper (70929-0002-1). 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 Antibe Beausenne Special Ampoule?

After cleansing, apply an appropriate amount of product on the face and neck area and gently pat for absorption. Use twice daily as the first step of your morning and night skin care regimen.

Which are Antibe Beausenne Special Ampoule UNII Codes?

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

Which are Antibe Beausenne Special Ampoule 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".