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  4. NDC Product Code: 66141-643 Thursday Plantation

NDC 66141-643 Thursday Plantation

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 66141-643?
  4. Thursday Plantation Uses
  5. Active Ingredients UNII Codes
  6. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
66141-643
Proprietary Name:
Thursday Plantation
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Integria Healthcare Ballina
Labeler Code:
66141
Product Label ID:
94acf69b-6ddc-4c85-857b-4c61e197cba9
Start Marketing Date: [9]
03-01-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 66141-643-50

Package Description: 100 g in 1 TUBE

Product Details

What is NDC 66141-643?

The NDC code 66141-643 is assigned by the FDA to the product Thursday Plantation which is product labeled by Integria Healthcare Ballina. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66141-643-50 100 g in 1 tube . 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 Thursday Plantation?

Uses:  minor burns, sunburn, minor skin irritations, scratches, dry skin, reduces inflammation

Which are Thursday Plantation UNII Codes?

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

  • AUSTRALIAN TEA TREE OIL (UNII: VIF565UC2G)
  • AUSTRALIAN TEA TREE OIL (UNII: VIF565UC2G) (Active Moiety)

What is the NDC to RxNorm Crosswalk for Thursday Plantation?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* 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".