1. Home
  2. Labeler Index
  3. Fujian Meigulin Bio-technique Co., Ltd.
  4. NDC Product Code: 70876-002 Tea Tree Oil

NDC 70876-002 Tea Tree Oil

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70876-002?
  4. Tea Tree Oil 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:
70876-002
Proprietary Name:
Tea Tree Oil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fujian Meigulin Bio-technique Co., Ltd.
Labeler Code:
70876
Product Label ID:
3b755c27-fc1d-6907-e054-00144ff8d46c
Start Marketing Date: [9]
08-18-2016
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70876-002-01

Package Description: 1 BOTTLE in 1 BOX / 10 g in 1 BOTTLE

Product Details

What is NDC 70876-002?

The NDC code 70876-002 is assigned by the FDA to the product Tea Tree Oil which is product labeled by Fujian Meigulin Bio-technique Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70876-002-01 1 bottle in 1 box / 10 g 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 Tea Tree Oil?

Apply to the affected area,use sparingly by drop,children under 12 years of age :consult a doctor.

Which are Tea Tree Oil UNII Codes?

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

  • MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
  • MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) (Active Moiety)

Which are Tea Tree Oil 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".