NDC 57955-2800 Aversion To Change
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57955 - King Bio Inc.
- 57955-2800 - Aversion To Change
Product Packages
NDC Code 57955-2800-2
Package Description: 59 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 57955-2800?
What are the uses for Aversion To Change?
Which are Aversion To Change UNII Codes?
The UNII codes for the active ingredients in this product are:
- MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB)
- MAHONIA AQUIFOLIUM ROOT BARK (UNII: VZJ9F3C3SB) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- GUAIACUM OFFICINALE RESIN (UNII: N0K2Z502R6)
- GUAIACUM OFFICINALE RESIN (UNII: N0K2Z502R6) (Active Moiety)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG)
- JUGLANS REGIA FLOWERING TOP (UNII: 3BA2N709NG) (Active Moiety)
- POTASSIUM DICHROMATE (UNII: T4423S18FM)
- DICHROMATE ION (UNII: 9LKY4BFN2V) (Active Moiety)
- LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY)
- LONICERA CAPRIFOLIUM FLOWERING TOP (UNII: 1X0T378SXY) (Active Moiety)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV)
- DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- VIOLA ODORATA (UNII: AET12U8B74)
- VIOLA ODORATA (UNII: AET12U8B74) (Active Moiety)
Which are Aversion To Change 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- 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".