1. Home
  2. Labeler Index
  3. Nuggela & Sule Sl
  4. NDC Product Code: 71578-006 Hair Treatment Premium

NDC 71578-006 Hair Treatment Premium

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71578-006?
  4. Hair Treatment Premium 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:
71578-006
Proprietary Name:
Hair Treatment Premium
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nuggela & Sule Sl
Labeler Code:
71578
Product Label ID:
55920970-7aea-4df8-e054-00144ff8d46c
Start Marketing Date: [9]
07-27-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71578-006-01

Package Description: 250 mL in 1 BOTTLE

Product Details

What is NDC 71578-006?

The NDC code 71578-006 is assigned by the FDA to the product Hair Treatment Premium which is product labeled by Nuggela & Sule Sl. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71578-006-01 250 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 Hair Treatment Premium?

Pour shampoo unto your hand and rub your palms to emulsify it, apply on hair and scalp, massage evenly for a few minutes and rinse throughly with water. Repeat to enhance its effectsFor easier combining and better results, combine the product with Nuggela & Sule Extreme conditioner.

Which are Hair Treatment Premium UNII Codes?

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

Which are Hair Treatment Premium 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".