NDC 57520-0144 Neuro Balance Pro
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apothecacompany
- 57520-0144 - Neuro Balance Pro
Product Packages
NDC Code 57520-0144-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 57520-0144?
What are the uses for Neuro Balance Pro?
Which are Neuro Balance Pro UNII Codes?
The UNII codes for the active ingredients in this product are:
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) (Active Moiety)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- GLUTAMIC ACID (UNII: 3KX376GY7L) (Active Moiety)
- NOREPINEPHRINE (UNII: X4W3ENH1CV)
- NOREPINEPHRINE (UNII: X4W3ENH1CV) (Active Moiety)
- ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R)
- ACETYLCHOLINE (UNII: N9YNS0M02X) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- SEROTONIN (UNII: 333DO1RDJY)
- SEROTONIN (UNII: 333DO1RDJY) (Active Moiety)
- THYROID (UNII: 0B4FDL9I6P)
- THYROID (UNII: 0B4FDL9I6P) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (Active Moiety)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)
- LEVODOPA (UNII: 46627O600J)
- LEVODOPA (UNII: 46627O600J) (Active Moiety)
Which are Neuro Balance Pro 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".