1. Home
  2. Labeler Index
  3. Kyron Laboratories (pty) Ltd
  4. NDC Product Code: 70674-001 Arnica Ice Cooling

NDC 70674-001 Arnica Ice Cooling

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70674-001?
  4. Arnica Ice Cooling 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:
70674-001
Proprietary Name:
Arnica Ice Cooling
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kyron Laboratories (pty) Ltd
Labeler Code:
70674
Product Label ID:
8151ecdf-ca41-420e-8e4c-196c66350314
Start Marketing Date: [9]
05-23-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70674-001-01

Package Description: 475 mg in 1 JAR

NDC Code 70674-001-02

Package Description: 100 mg in 1 PACKAGE

Product Details

What is NDC 70674-001?

The NDC code 70674-001 is assigned by the FDA to the product Arnica Ice Cooling which is product labeled by Kyron Laboratories (pty) Ltd. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70674-001-01 475 mg in 1 jar , 70674-001-02 100 mg in 1 package . 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 Arnica Ice Cooling?

Indications and usage

Which are Arnica Ice Cooling UNII Codes?

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

Which are Arnica Ice Cooling 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".