NDC 11822-2235 Cairina Moschata Heart/liver Autolysate

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
11822-2235
Proprietary Name:
Cairina Moschata Heart/liver Autolysate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid Hdgrts Corp
Labeler Code:
11822
Start Marketing Date: [9]
12-13-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11822-2235-3

Package Description: 30 VIAL in 1 CARTON / 200 PELLET in 1 VIAL

Product Details

What is NDC 11822-2235?

The NDC code 11822-2235 is assigned by the FDA to the product Cairina Moschata Heart/liver Autolysate which is product labeled by Rite Aid Hdgrts Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-2235-3 30 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.

[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".