1. Home
  2. Labeler Index
  3. The Greenery Lab
  4. NDC Product Code: 72636-101 Perilla Fo Ti Conditioner

NDC 72636-101 Perilla Fo Ti Conditioner

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72636-101?
  5. Perilla Fo Ti Conditioner Uses
  6. Active Ingredients UNII Codes
  7. 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:
72636-101
Proprietary Name:
Perilla Fo Ti Conditioner
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Greenery Lab
Labeler Code:
72636
Product Label ID:
798c853c-16a5-8502-e053-2a91aa0a6532
Start Marketing Date: [9]
10-31-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Code Structure Chart

Product Details

What is NDC 72636-101?

The NDC code 72636-101 is assigned by the FDA to the product Perilla Fo Ti Conditioner which is product labeled by The Greenery Lab. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72636-101-02 1 bottle, pump in 1 box / 500 g in 1 bottle, pump (72636-101-01). 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 Perilla Fo Ti Conditioner?

Use after shampooing. Apply the conditioner on scalp and along the length of your hair tips. Leave in for at least 2 minutes. Rinse thoroughly with water. Product does not lather. For best results use with Perilla Fo-ti Shampoo.

Which are Perilla Fo Ti Conditioner UNII Codes?

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

Which are Perilla Fo Ti Conditioner 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".