NDC 63776-450 Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63776 - Viatrexx Bio Incorporated
- 63776-450 - Relief
Product Packages
NDC Code 63776-450-14
Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 63776-450?
What are the uses for Relief?
Which are Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R)
- ACETYLCHOLINE (UNII: N9YNS0M02X) (Active Moiety)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
- CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
- CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)
- HISTAMINE (UNII: 820484N8I3)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
- HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
- HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
- SEROTONIN (UNII: 333DO1RDJY)
- SEROTONIN (UNII: 333DO1RDJY) (Active Moiety)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S)
- ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S) (Active Moiety)
Which are Relief 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:
- ALCOHOL (UNII: 3K9958V90M)
- 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".