1. Home
  2. Labeler Index
  3. Feelxo
  4. NDC Product Code: 71694-0001 Pore Care Lotus Mask

NDC 71694-0001 Pore Care Lotus Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71694-0001?
  4. Pore Care Lotus Mask 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:
71694-0001
Proprietary Name:
Pore Care Lotus Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Feelxo
Labeler Code:
71694
Product Label ID:
57de50d3-c9f6-5576-e053-2a91aa0a7937
Start Marketing Date: [9]
08-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 71694-0001?

The NDC code 71694-0001 is assigned by the FDA to the product Pore Care Lotus Mask which is product labeled by Feelxo. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71694-0001-1 25 ml in 1 pouch . 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 Pore Care Lotus Mask?

1. Cleanse and tone the skin.Unfold the mask and carefully adjust it onto your face.Leave the mask on your face for 15~20 minutes for best outcome.Remove the mask and gently massage excess serum for better absorption.

Which are Pore Care Lotus Mask UNII Codes?

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

Which are Pore Care Lotus Mask 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".