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NDC 72194-010 Fjell Mask Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72194-010?
  4. Fjell Mask Pack 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:
72194-010
Proprietary Name:
Fjell Mask Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fjell Inc.
Labeler Code:
72194
Product Label ID:
9de27a47-1340-496a-aa64-998b841e56bc
Start Marketing Date: [9]
03-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 72194-010?

The NDC code 72194-010 is assigned by the FDA to the product Fjell Mask Pack which is product labeled by Fjell Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72194-010-02 1 container in 1 carton / 150 ml in 1 container (72194-010-01). 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 Fjell Mask Pack?

Directions:For best results, clean and dry skin before use. Test on a small area for allergies before use. Discontinue if irritation occurs. Apply a thick layer of the mask onto the face and neck avoiding the delicate eye area. Let the mask sit for 20~30 minutes depending on your skin type. Thoroughly rinse with warm water.

Which are Fjell Mask Pack UNII Codes?

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

Which are Fjell Mask Pack 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".