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  4. NDC Product Code: 69346-0001 Wellage Family Mask Small

NDC 69346-0001 Wellage Family Mask Small

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69346-0001?
  4. Wellage Family Mask Small 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:
69346-0001
Proprietary Name:
Wellage Family Mask Small
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hugel Pharma Co.,ltd
Labeler Code:
69346
Product Label ID:
3c48b7cd-8424-7292-e054-00144ff88e88
Start Marketing Date: [9]
09-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69346-0001?

The NDC code 69346-0001 is assigned by the FDA to the product Wellage Family Mask Small which is product labeled by Hugel Pharma Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69346-0001-3 10 pouch in 1 package / 20 ml in 1 pouch (69346-0001-1). 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 Wellage Family Mask Small?

Remove mask from pouch and place on face for 15-20 minutes.Pat in remaining essence to absorb into skin. *Masks should be stored lying flat to ensure essence is evenly distributed throughout the sheets.

Which are Wellage Family Mask Small UNII Codes?

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

Which are Wellage Family Mask Small 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".