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  4. NDC Product Code: 59672-0032 Arnica

NDC 59672-0032 Arnica

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 59672-0032?
  5. Arnica Uses
  6. Active Ingredients UNII Codes
  7. 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:
59672-0032
Proprietary Name:
Arnica
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lc Industries
Labeler Code:
59672
Product Label ID:
8a77c539-4dc1-4859-89f9-4fd17a8d4214
Start Marketing Date: [9]
03-07-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
ML
Score:
1

Code Structure Chart

Product Details

What is NDC 59672-0032?

The NDC code 59672-0032 is assigned by the FDA to the product Arnica which is product labeled by Lc Industries. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59672-0032-0 1 blister pack in 1 box / 32 tablet in 1 blister pack. 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?

AgeDoseAdults and Children 2 years and overChew two tablets after exercise or physical activity - work or sports. Best taken separately from meals. Can be taken with all other types of medication.Under 2 yearsAsk a doctor.

Which are Arnica UNII Codes?

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

Which are Arnica 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".