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  4. NDC Product Code: 72729-060 Cytokine 8

NDC 72729-060 Cytokine 8

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 72729-060?
  4. Cytokine 8 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:
72729-060
Proprietary Name:
Cytokine 8
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Woorhi Mechatronics Co., Ltd.
Labeler Code:
72729
Product Label ID:
987d5d86-70f7-476f-8e55-0ed747072b95
Start Marketing Date: [9]
02-01-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 72729-060?

The NDC code 72729-060 is assigned by the FDA to the product Cytokine 8 which is product labeled by Woorhi Mechatronics Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72729-060-01 1 kit in 1 carton * 30 ml in 1 bottle, spray * 30 ml in 1 bottle. 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 Cytokine 8?

[CLEAN FOLLICLE SPRAY]■ Before using, shaking it thoroughly.■ Spray it onto the scalp 3~5 times every morning/evening and massage it for absorption.[CLEAN FOLLICLE TONIC]■ Before using, shaking it thoroughly.■ Pour it into enclosed CYTOKINE-8 powder solution and mix together.■ Apply on scalp and massage on the scalp area to be absorbed.

Which are Cytokine 8 UNII Codes?

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

Which are Cytokine 8 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".