NDC 69346-0003 Wellage Black Aqua Roll 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:
69346-0003
Proprietary Name:
Wellage Black Aqua Roll Mask Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hugel Pharma Co.,ltd
Labeler Code:
69346
Start Marketing Date: [9]
09-08-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69346-0003-1

Package Description: 10 POUCH in 1 CYLINDER / 25 mL in 1 POUCH

Product Details

What is NDC 69346-0003?

The NDC code 69346-0003 is assigned by the FDA to the product Wellage Black Aqua Roll Mask Pack 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 69346-0003-1 10 pouch in 1 cylinder / 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 Wellage Black Aqua Roll Mask Pack?

Remove mask. Hold the rod horizontally and align it to the center of the forehead.Use free hand to unravel the mask sheet from the rod and position mask on face.Peel off mask in 10-20 minutes and pat in remaining essence to absorb into skin.

Which are Wellage Black Aqua Roll Mask Pack UNII Codes?

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

Which are Wellage Black Aqua Roll 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".