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  4. NDC Product Code: 71975-050 Ultra V Aqua Shine Mask

NDC 71975-050 Ultra V Aqua Shine Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71975-050?
  4. Ultra V Aqua Shine 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:
71975-050
Proprietary Name:
Ultra V Aqua Shine Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Ultra V Co., Ltd
Labeler Code:
71975
Product Label ID:
8512733d-4c34-47ef-8195-9071ba06d753
Start Marketing Date: [9]
01-02-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71975-050-02

Package Description: 10 POUCH in 1 CARTON / 25 mL in 1 POUCH (71975-050-01)

Product Details

What is NDC 71975-050?

The NDC code 71975-050 is assigned by the FDA to the product Ultra V Aqua Shine Mask which is product labeled by Ultra V Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71975-050-02 10 pouch in 1 carton / 25 ml in 1 pouch (71975-050-01). 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 Ultra V Aqua Shine Mask?

Directions: Clean up your face using skin-toner after washing face. Place mask-sheet from the eye line and fix it along with face line downward. Keep staying 10 to 20 min and take it off from the face. Remained essential liquid on face needs to be absorbed using finger tip.

Which are Ultra V Aqua Shine Mask UNII Codes?

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

Which are Ultra V Aqua Shine 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:

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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".