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  4. NDC Product Code: 81817-201 Zenotri Follicle Shampoo.

NDC 81817-201 Zenotri Follicle Shampoo.

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 81817-201?
  4. Zenotri Follicle Shampoo. 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:
81817-201
Proprietary Name:
Zenotri Follicle Shampoo.
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Chromach Co., Ltd.
Labeler Code:
81817
Product Label ID:
c0dc4271-557e-6c75-e053-2a95a90a02eb
Start Marketing Date: [9]
04-26-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 81817-201?

The NDC code 81817-201 is assigned by the FDA to the product Zenotri Follicle Shampoo. which is product labeled by Chromach Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 81817-201-02 1 bottle, plastic in 1 carton / 300 ml in 1 bottle, plastic (81817-201-01). 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 Zenotri Follicle Shampoo.?

For best results use at least twice a week or as directed by a doctorUse once a day (morning or evening) with warm water and thoroughly soak the hair and scalp. Massage the hair and scalp thoroughly with 3~5ml, wait for more than 3 minutes as Foaming state, and rinse thoroughly with water.

Which are Zenotri Follicle Shampoo. UNII Codes?

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

Which are Zenotri Follicle Shampoo. 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".