NDC 57955-5015 Attention And Learning Enhancement
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-5015 - Attention And Learning Enhancement
Product Packages
NDC Code 57955-5015-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-5015?
What are the uses for Attention And Learning Enhancement?
Which are Attention And Learning Enhancement UNII Codes?
The UNII codes for the active ingredients in this product are:
- 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)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
Which are Attention And Learning Enhancement 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)
* 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".