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  4. NDC Product Code: 68428-087 Calendula Officinalis Kit Refill

NDC 68428-087 Calendula Officinalis Kit Refill

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68428-087?
  5. Calendula Officinalis 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:
68428-087
Proprietary Name:
Calendula Officinalis 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:
3c461e1c-e1b2-4f8f-9845-a76532c8985b
Start Marketing Date: [9]
10-09-2009
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)

Product Packages

NDC Code 68428-087-01

Package Description: 750 PELLET in 1 VIAL, GLASS

Product Details

What is NDC 68428-087?

The NDC code 68428-087 is assigned by the FDA to the product Calendula Officinalis 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 68428-087-01 750 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 Calendula Officinalis Kit Refill?

Indications: CALENDULA OFFICINALIS     Wounds

Which are Calendula Officinalis Kit Refill UNII Codes?

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

  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
  • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)

Which are Calendula Officinalis 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".