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  4. NDC Product Code: 69320-100 Arhtri Plus

NDC 69320-100 Arhtri Plus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69320-100?
  4. Arhtri Plus Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
69320-100
Proprietary Name:
Arhtri Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Distributions Ar?mes D`espagne Enr
Labeler Code:
69320
Product Label ID:
da7808fa-a95e-4369-b6ac-c22a46c07291
Start Marketing Date: [9]
10-30-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69320-100-01

Package Description: 150 g in 1 BOTTLE, SPRAY

Product Details

What is NDC 69320-100?

The NDC code 69320-100 is assigned by the FDA to the product Arhtri Plus which is product labeled by Distributions Ar?mes D`espagne Enr. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69320-100-01 150 g in 1 bottle, spray . 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 Arhtri Plus?

For adults and children 2 years of age and older: Shake well before use. Apply to the affected area not more than 3-4 times daily. Allow absorption to occur naturally for maximum penetration. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a health care practitioner.

Which are Arhtri Plus UNII Codes?

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

Which are Arhtri Plus 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:

What is the NDC to RxNorm Crosswalk for Arhtri Plus?

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:
  • RxCUI: 1592734 - menthol 2.5 % / eucalyptus oil 0.72 % / clove oil 0.25 % Topical Spray
  • RxCUI: 1592734 - clove oil 2.5 MG/ML / Eucalyptus oil 7.2 MG/ML / menthol 25 MG/ML Topical Spray
  • RxCUI: 1592734 - clove oil 0.25 % / eucalyptus oil 0.72 % / menthol 2.5 % Topical Spray

* 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".