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  4. NDC Product Code: 50126-001

NDC 50126-001

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 50126-001?
  4. Uses
  5. Active 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:
50126-001
Proprietary Name:
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Advanced Natural Solutions
Labeler Code:
50126
Product Label ID:
f5849afe-d254-4720-8519-19956df18ae7
Start Marketing Date: [9]
10-20-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 50126-001-08

Package Description: 237 mL in 1 BOTTLE

Product Details

What is NDC 50126-001?

The NDC code 50126-001 is assigned by the FDA to the product which is product labeled by Advanced Natural Solutions. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50126-001-08 237 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 ?

Directions:  Adult and children 6 months of age or older:Shake wellApply liberally to wet hair and entire scalp, starting at the nape of the neck and behind ears working forwardMassage in thoroughly until entire head is covered; to be effective, all lice and nits must come in full contact with the productLeave in hair for 15 minutesUse comb to remove all lice and eggsRinse hair thoroughly with warm water Repeat as necessaryUses:  Homeopathic remedy for treatment of head lice as per Materia Medica.

Which are UNII Codes?

The UNII codes for the active 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".