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  4. NDC Product Code: 73456-020 Ambling Plant Probiotics Aqua Role Moisturizing

NDC 73456-020 Ambling Plant Probiotics Aqua Role Moisturizing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73456-020?
  4. Ambling Plant Probiotics Aqua Role Moisturizing 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:
73456-020
Proprietary Name:
Ambling Plant Probiotics Aqua Role Moisturizing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amtixbio Co., Ltd.
Labeler Code:
73456
Product Label ID:
d0982c95-51a1-4110-85c7-9100002e238f
Start Marketing Date: [9]
10-01-2019
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 73456-020?

The NDC code 73456-020 is assigned by the FDA to the product Ambling Plant Probiotics Aqua Role Moisturizing which is product labeled by Amtixbio Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73456-020-02 1 container in 1 carton / 50 ml in 1 container (73456-020-01). 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 Ambling Plant Probiotics Aqua Role Moisturizing?

Directions:After cleansing or applying our ampoule, take an appropriate amount of this product and spread evenly on the skin.*Over time, there may be sedimentation and slight discoloration due to the inclusion of natural ingredients, but there is no abnormality in the product.

Which are Ambling Plant Probiotics Aqua Role Moisturizing UNII Codes?

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

Which are Ambling Plant Probiotics Aqua Role Moisturizing 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".