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  4. NDC Product Code: 82343-020 Dr. Scalp Spicule Complex

NDC 82343-020 Dr. Scalp Spicule Complex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82343-020?
  4. Dr. Scalp Spicule Complex 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:
82343-020
Proprietary Name:
Dr. Scalp Spicule Complex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Dr Scalp Co., Ltd.
Labeler Code:
82343
Product Label ID:
d8ffb86d-2562-4da0-8e75-6acc1c5039d0
Start Marketing Date: [9]
10-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 82343-020?

The NDC code 82343-020 is assigned by the FDA to the product Dr. Scalp Spicule Complex which is product labeled by Dr Scalp Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82343-020-02 1 container in 1 carton / 70 ml in 1 container (82343-020-01). 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. Scalp Spicule Complex?

■ Apply on scalp where hair loss treatment is urgently needed.■ For best results use at least once a day

Which are Dr. Scalp Spicule Complex UNII Codes?

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

Which are Dr. Scalp Spicule Complex 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".