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  4. NDC Product Code: 81710-110 Dr.different Vitaacnal Tx Capsule Serum

NDC 81710-110 Dr.different Vitaacnal Tx Capsule Serum

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81710-110?
  4. Dr.different Vitaacnal Tx Capsule Serum 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:
81710-110
Proprietary Name:
Dr.different Vitaacnal Tx Capsule Serum
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dareun Cosmetics Co., Ltd.
Labeler Code:
81710
Product Label ID:
2f3604f8-8567-4bd8-934d-02766db560b7
Start Marketing Date: [9]
12-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81710-110-02

Package Description: 1 CONTAINER in 1 CARTON / 30 mL in 1 CONTAINER (81710-110-01)

Product Details

What is NDC 81710-110?

The NDC code 81710-110 is assigned by the FDA to the product Dr.different Vitaacnal Tx Capsule Serum which is product labeled by Dareun Cosmetics Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81710-110-02 1 container in 1 carton / 30 ml in 1 container (81710-110-01). 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 Dr.different Vitaacnal Tx Capsule Serum?

After cleansing, take out an adequate amount on a hand, gently apply then dab to help the skin absorb.

Which are Dr.different Vitaacnal Tx Capsule Serum UNII Codes?

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

Which are Dr.different Vitaacnal Tx Capsule Serum 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".