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  4. NDC Product Code: 72470-050 Village 11 Factory Relax Day Aha Exfoliating Body

NDC 72470-050 Village 11 Factory Relax Day Aha Exfoliating Body

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72470-050?
  4. Village 11 Factory Relax Day Aha Exfoliating Body 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:
72470-050
Proprietary Name:
Village 11 Factory Relax Day Aha Exfoliating Body
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Pfd Co.,ltd.
Labeler Code:
72470
Product Label ID:
df4e7d6a-ebca-45c1-b2f3-e5649120fd73
Start Marketing Date: [9]
11-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 72470-050?

The NDC code 72470-050 is assigned by the FDA to the product Village 11 Factory Relax Day Aha Exfoliating Body which is product labeled by Pfd Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72470-050-02 1 container in 1 carton / 300 g in 1 container (72470-050-01). 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 Village 11 Factory Relax Day Aha Exfoliating Body?

■ Take an appropriate amount on clean body skin and apply gently letting it absorb.■ This product is rich in AHA and a patch test is recommended before use.

Which are Village 11 Factory Relax Day Aha Exfoliating Body UNII Codes?

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

Which are Village 11 Factory Relax Day Aha Exfoliating Body 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".