NDC 71820-0001 Anti Aging Hydrogel Mask Pack

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71820-0001
Proprietary Name:
Anti Aging Hydrogel Mask Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mask Factory
Labeler Code:
71820
Start Marketing Date: [9]
10-21-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71820-0001-1

Package Description: 30 g in 1 PACKAGE

Product Details

What is NDC 71820-0001?

The NDC code 71820-0001 is assigned by the FDA to the product Anti Aging Hydrogel Mask Pack which is product labeled by Mask Factory. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71820-0001-1 30 g in 1 package . 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 Anti Aging Hydrogel Mask Pack?

Gently apply the mask to fit your faceleave the mask on yor face for 20~30 minutesremove the mask and lightly pat remaining

Which are Anti Aging Hydrogel Mask Pack UNII Codes?

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

Which are Anti Aging Hydrogel 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:

* 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".