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  4. NDC Product Code: 70514-0001 Pearl Rewhite Transfusion Dna Kit

NDC 70514-0001 Pearl Rewhite Transfusion Dna Kit

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70514-0001?
  4. Pearl Rewhite Transfusion Dna Kit 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:
70514-0001
Proprietary Name:
Pearl Rewhite Transfusion Dna Kit
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Karatica Co., Ltd
Labeler Code:
70514
Product Label ID:
5f2e1a9c-6797-02ef-e053-2a91aa0ab806
Start Marketing Date: [9]
11-29-2017
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 70514-0001?

The NDC code 70514-0001 is assigned by the FDA to the product Pearl Rewhite Transfusion Dna Kit which is product labeled by Karatica Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70514-0001-1 22 ml in 1 ampule . 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 Pearl Rewhite Transfusion Dna Kit?

Take appropriate amount and evenly apply it to the skinOpen the lid of the vial and remove aluminum thread carefullyInsert vial in serter in the vial.Drop the fomula on wrinkles around eyes and mouth and the entire face. Then use your fingertips to help formula to be absorbed into the skin.

Which are Pearl Rewhite Transfusion Dna Kit UNII Codes?

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

Which are Pearl Rewhite Transfusion Dna Kit 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".