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  4. NDC Product Code: 68428-163 Spigelia Anthelmia Kit Refill

NDC 68428-163 Spigelia Anthelmia Kit Refill

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68428-163?
  5. Spigelia Anthelmia Kit Refill 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:
68428-163
Proprietary Name:
Spigelia Anthelmia Kit Refill
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Washington Homeopathic Products
Labeler Code:
68428
Product Label ID:
902b04f2-5151-4d4b-b4ec-760b51102fd4
Start Marketing Date: [9]
10-09-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)

Code Structure Chart

Product Details

What is NDC 68428-163?

The NDC code 68428-163 is assigned by the FDA to the product Spigelia Anthelmia Kit Refill which is product labeled by Washington Homeopathic Products. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68428-163-01 750 pellet in 1 vial, glass . 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 Spigelia Anthelmia Kit Refill?

Indications: SPIGELIA ANTHELMIA   Headache

Which are Spigelia Anthelmia Kit Refill UNII Codes?

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

Which are Spigelia Anthelmia Kit Refill 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:

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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".