NDC 63083-2097 Adjustment Disorders Formula 2097
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2097 - Adjustment Disorders Formula
Product Packages
NDC Code 63083-2097-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2097?
What are the uses for Adjustment Disorders Formula 2097?
Which are Adjustment Disorders Formula 2097 UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIEFFENBACHIA SEGUINE WHOLE (UNII: 01800C6E6B)
- DIEFFENBACHIA SEGUINE WHOLE (UNII: 01800C6E6B) (Active Moiety)
- ANTIPYRINE (UNII: T3CHA1B51H)
- ANTIPYRINE (UNII: T3CHA1B51H) (Active Moiety)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC)
- ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (Active Moiety)
- DIGITALIS (UNII: F1T8QT9U8B)
- DIGITALIS (UNII: F1T8QT9U8B) (Active Moiety)
- NITROGLYCERIN (UNII: G59M7S0WS3)
- NITROGLYCERIN (UNII: G59M7S0WS3) (Active Moiety)
- XEROPHYLLUM ASPHODELOIDES WHOLE (UNII: 9I4XB1GP2B)
- XEROPHYLLUM ASPHODELOIDES WHOLE (UNII: 9I4XB1GP2B) (Active Moiety)
- AGAVE ATROVIRENS TOP (UNII: E7M31AEM0L)
- AGAVE ATROVIRENS TOP (UNII: E7M31AEM0L) (Active Moiety)
- WOOD CREOSOTE (UNII: 3JYG22FD73)
- WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- RABIES VIRUS (UNII: I0V66KI1LD)
- RABIES VIRUS (UNII: I0V66KI1LD) (Active Moiety)
Which are Adjustment Disorders Formula 2097 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)
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[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".