NDC 63083-2009 Anti-stress Drops 2009
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2009 - Anti-stress Drops
Product Packages
NDC Code 63083-2009-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2009?
What are the uses for Anti-stress Drops 2009?
Which are Anti-stress Drops 2009 UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW)
- ARTEMISIA ANNUA FLOWERING TOP (UNII: 0UQK6O82OW) (Active Moiety)
- ROYAL JELLY (UNII: L497I37F0C)
- ROYAL JELLY (UNII: L497I37F0C) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- CITRUS AURANTIUM FRUIT RIND (UNII: 055456JHI7)
- CITRUS AURANTIUM FRUIT RIND (UNII: 055456JHI7) (Active Moiety)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K)
- STRYCHNOS IGNATII SEED (UNII: 1NM3M2487K) (Active Moiety)
- NEUROTENSIN (UNII: XHB61LG5QS)
- NEUROTENSIN (UNII: XHB61LG5QS) (Active Moiety)
Which are Anti-stress Drops 2009 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".