NDC 43857-0512 Cardiotone
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0512 - Cardiotone
Product Packages
NDC Code 43857-0512-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43857-0512?
What are the uses for Cardiotone?
Which are Cardiotone UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK)
- SELENICEREUS GRANDIFLORUS STEM (UNII: 7114SV0MYK) (Active Moiety)
- CONVALLARIA MAJALIS (UNII: QHH4HVF5QE)
- CONVALLARIA MAJALIS (UNII: QHH4HVF5QE) (Active Moiety)
- PORK HEART (UNII: X876KJM95L)
- PORK HEART (UNII: X876KJM95L) (Active Moiety)
- MAGNESIUM GLUCONATE (UNII: T42NAD2KHC)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- POTASSIUM GLUCONATE (UNII: 12H3K5QKN9)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (Active Moiety)
- STROPHANTHUS HISPIDUS SEED (UNII: MO892VI77K)
- STROPHANTHUS HISPIDUS SEED (UNII: MO892VI77K) (Active Moiety)
- ADONIS VERNALIS (UNII: DX3ZNI25WK)
- ADONIS VERNALIS (UNII: DX3ZNI25WK) (Active Moiety)
- DIGITALIS (UNII: F1T8QT9U8B)
- DIGITALIS (UNII: F1T8QT9U8B) (Active Moiety)
Which are Cardiotone 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* Please review the disclaimer below.
[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".