NDC 81710-070 Dr.different Vitaacnal Tx Night

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:
81710-070
Proprietary Name:
Dr.different Vitaacnal Tx Night
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dareun Cosmetics Co., Ltd.
Labeler Code:
81710
Start Marketing Date: [9]
04-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 81710-070-02

Package Description: 1 TUBE in 1 CARTON / 20 g in 1 TUBE (81710-070-01)

Product Details

What is NDC 81710-070?

The NDC code 81710-070 is assigned by the FDA to the product Dr.different Vitaacnal Tx Night 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 81710-070-02 1 tube in 1 carton / 20 g in 1 tube (81710-070-01). 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 Night?

This product is for night use. At the final step of your nightly skincare routine or before going to bed, gently apply an adequate amount across your entire face.*If you are trying this product for the first time, we recommend you to test a small amount before use.

Which are Dr.different Vitaacnal Tx Night UNII Codes?

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

  • CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)
  • CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4) (Active Moiety)

Which are Dr.different Vitaacnal Tx Night 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".