1. Home
  2. Labeler Index
  3. My Import Usa Inc
  4. NDC Product Code: 51628-0002 Xtracare Anti-dandruff Hair Cleanse For Normal Hair

NDC 51628-0002 Xtracare Anti-dandruff Hair Cleanse For Normal Hair

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51628-0002?
  4. Xtracare Anti-dandruff Hair Cleanse For Normal Hair 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:
51628-0002
Proprietary Name:
Xtracare Anti-dandruff Hair Cleanse For Normal Hair
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
My Import Usa Inc
Labeler Code:
51628
Product Label ID:
ab084d44-dfb8-4cde-bfa1-17d72cce686e
Start Marketing Date: [9]
10-09-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 51628-0002?

The NDC code 51628-0002 is assigned by the FDA to the product Xtracare Anti-dandruff Hair Cleanse For Normal Hair which is product labeled by My Import Usa Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51628-0002-1 400 mg 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 Xtracare Anti-dandruff Hair Cleanse For Normal Hair?

Uses helps prevent recurrence of flaking and itching associated with dandruff.Gentle enough for everyday use. For best results, use with XtraCare nourishing coconut & shea butter conditioner.

Which are Xtracare Anti-dandruff Hair Cleanse For Normal Hair UNII Codes?

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

Which are Xtracare Anti-dandruff Hair Cleanse For Normal Hair 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".