NDC 50845-0245 Vital Immune Booster
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50845 - Liddell Laboratories, Inc.
- 50845-0245 - Vital Immune Booster
Product Packages
NDC Code 50845-0245-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 50845-0245?
What are the uses for Vital Immune Booster?
Which are Vital Immune Booster UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- BORATE ION (UNII: 44OAE30D22) (Active Moiety)
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3)
- HELIANTHEMUM CANADENSE (UNII: 46G3W789Q3) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- GALIUM APARINE (UNII: Z4B6561488)
- GALIUM APARINE (UNII: Z4B6561488) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT)
- SUS SCROFA PITUITARY GLAND (UNII: L0PFEMQ1DT) (Active Moiety)
- NITRIC ACID (UNII: 411VRN1TV4)
- NITRIC ACID (UNII: 411VRN1TV4) (Active Moiety)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG)
- PHYTOLACCA AMERICANA ROOT (UNII: 11E6VI8VEG) (Active Moiety)
- SULFUR IODIDE (UNII: L6L8KA2AA0)
- SULFUR IODIDE (UNII: L6L8KA2AA0) (Active Moiety)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397)
- THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (Active Moiety)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62)
- SUS SCROFA THYMUS (UNII: 7B69B0BD62) (Active Moiety)
Which are Vital Immune Booster 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
* 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".