NDC 63083-1011 Nightshade Mix 1011
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-1011 - Nightshade Mix
Product Packages
NDC Code 63083-1011-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-1011?
What are the uses for Nightshade Mix 1011?
Which are Nightshade Mix 1011 UNII Codes?
The UNII codes for the active ingredients in this product are:
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV)
- SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (Active Moiety)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
- BEEF LIVER (UNII: W8N8R55022)
- BEEF LIVER (UNII: W8N8R55022) (Active Moiety)
- CAPSICUM (UNII: 00UK7646FG)
- CAPSICUM (UNII: 00UK7646FG) (Active Moiety)
- EGGPLANT (UNII: W5K7RAS4VK)
- EGGPLANT (UNII: W5K7RAS4VK) (Active Moiety)
- PHYSALIS VIRGINIANA WHOLE (UNII: 270AG5WWGC)
- PHYSALIS VIRGINIANA WHOLE (UNII: 270AG5WWGC) (Active Moiety)
- CULTIVATED MUSHROOM (UNII: 54C8E6W6JY)
- CULTIVATED MUSHROOM (UNII: 54C8E6W6JY) (Active Moiety)
- MUSTARD GREENS (UNII: 5M338IN22E)
- MUSTARD GREENS (UNII: 5M338IN22E) (Active Moiety)
- PEPPERS (UNII: T5KDM4J239)
- PEPPERS (UNII: T5KDM4J239) (Active Moiety)
- POTATO (UNII: CFE1S8DYWD)
- POTATO (UNII: CFE1S8DYWD) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- TOMATO (UNII: Z4KHF2C175)
- TOMATO (UNII: Z4KHF2C175) (Active Moiety)
Which are Nightshade Mix 1011 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".