1. Home
  2. Labeler Index
  3. Mentor Lab
  4. NDC Product Code: 69961-040 Baramo For O Ily Scalp

NDC 69961-040 Baramo For O Ily Scalp

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69961-040?
  4. Baramo For O Ily Scalp 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:
69961-040
Proprietary Name:
Baramo For O Ily Scalp
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mentor Lab
Labeler Code:
69961
Product Label ID:
04c3daac-f2f4-4ccd-a4b5-16899767301d
Start Marketing Date: [9]
10-01-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 69961-040?

The NDC code 69961-040 is assigned by the FDA to the product Baramo For O Ily Scalp which is product labeled by Mentor Lab. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69961-040-02 1 bottle, pump in 1 carton / 300 ml in 1 bottle, pump (69961-040-01). 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 Baramo For O Ily Scalp?

This product is used as Purpose: purifies & nourishes hair and scalp

Which are Baramo For O Ily Scalp UNII Codes?

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

  • STYPHNOLOBIUM JAPONICUM FLOWER BUD (UNII: DES4RX1Z3E)
  • STYPHNOLOBIUM JAPONICUM FLOWER BUD (UNII: DES4RX1Z3E) (Active Moiety)

Which are Baramo For O Ily Scalp 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".