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  4. NDC Product Code: 70768-010 Black Cavidiol Mask

NDC 70768-010 Black Cavidiol Mask

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70768-010?
  4. Black Cavidiol 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:
70768-010
Proprietary Name:
Black Cavidiol Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Zemna Company Co., Ltd
Labeler Code:
70768
Product Label ID:
b752b665-b212-4caf-852f-dd873b7dd315
Start Marketing Date: [9]
05-01-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 70768-010?

The NDC code 70768-010 is assigned by the FDA to the product Black Cavidiol Mask which is product labeled by Zemna Company Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70768-010-02 1 pouch in 1 carton / 40 g in 1 pouch (70768-010-01). 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 Black Cavidiol Mask?

Indications & usage: 1) Apply a Black Cavidiol Mask onto clean skin and align it evenly onto the face. 2) Pull the bottom of the mask upward and align it evenly with the chin. 3) Remove after 10-20 minutes and lightly tap the skin until the serum is fully absorbed.

Which are Black Cavidiol Mask UNII Codes?

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

Which are Black Cavidiol 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".