1. Home
  2. Labeler Index
  3. Warsan Homoeopathic
  4. NDC Product Code: 69008-1001 Arthosan

NDC 69008-1001 Arthosan

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69008-1001?
  4. Arthosan 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.

Get all the details for National Drug Code (NDC) 69008-1001 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
69008-1001
Proprietary Name:
Arthosan
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Warsan Homoeopathic
Labeler Code:
69008
Product Label ID:
6593de91-905d-e547-e053-2991aa0ad131
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
02-19-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 69008-1001?

The NDC code 69008-1001 is assigned by the FDA to the product Arthosan which is product labeled by Warsan Homoeopathic. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69008-1001-9 240 ml 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 Arthosan?

Temporary relief from minor muscle and joint aches and pains including: low back pain, leg pain, joint pain, bruises, arthritis, stiffness.

Which are Arthosan UNII Codes?

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

  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
  • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW)
  • PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (Active Moiety)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
  • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
  • COMFREY ROOT (UNII: M9VVZ08EKQ)
  • COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
  • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6)
  • COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (Active Moiety)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U)
  • BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (Active Moiety)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N)
  • SOLANUM DULCAMARA TOP (UNII: KPS1B1162N) (Active Moiety)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
  • GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
  • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
  • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
  • GINGER (UNII: C5529G5JPQ)
  • GINGER (UNII: C5529G5JPQ) (Active Moiety)

Which are Arthosan 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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".