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  4. NDC Product Code: 63868-306 Cairina Moschata Heart/liver Autolysate

NDC 63868-306 Cairina Moschata Heart/liver Autolysate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63868-306?
  4. Cairina Moschata Heart/liver Autolysate 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 expired due to lack of listing certification.

Get all the details for National Drug Code (NDC) 63868-306 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:
63868-306
Proprietary Name:
Cairina Moschata Heart/liver Autolysate
Product Type: [3]
Labeler Name: [5]
Chain Drug Marketing Association Inc.
Labeler Code:
63868
Product Label ID:
d6eb1ed3-5a8f-4c4c-827e-8ac53ad536b7
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
08-01-2021
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
U
Code Navigator:

Code Structure Chart

Product Details

What is NDC 63868-306?

The NDC code 63868-306 is assigned by the FDA to the product Cairina Moschata Heart/liver Autolysate which is product labeled by Chain Drug Marketing Association Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63868-306-06 6 vial in 1 carton / 200 pellet in 1 vial. 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 Cairina Moschata Heart/liver Autolysate?

Adults and children 2 years of age and older:Dissolve entire contents of one tube in the mouth every 6 hours, up to 3 times a dayChildren under 2 years of age: Ask a doctor.

Which are Cairina Moschata Heart/liver Autolysate UNII Codes?

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

  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY)
  • CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE (UNII: RN2HC612GY) (Active Moiety)

Which are Cairina Moschata Heart/liver Autolysate 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.

[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".