NDC 50181-0028 Biotox VI
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50181 - The Wellness Center For Research And Education, Inc.
- 50181-0028 - Biotox
Product Packages
NDC Code 50181-0028-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50181-0028?
What are the uses for Biotox VI?
Which are Biotox VI UNII Codes?
The UNII codes for the active ingredients in this product are:
- HORSERADISH (UNII: 8DS6G120HJ)
- HORSERADISH (UNII: 8DS6G120HJ) (Active Moiety)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3)
- BOS TAURUS SPLEEN (UNII: 190Q9MB3U3) (Active Moiety)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8)
- BOS TAURUS THYMUS (UNII: 8XEJ88V2T8) (Active Moiety)
- INFLUENZA A VIRUS (UNII: R9HH0NDE2E)
- INFLUENZA A VIRUS (UNII: R9HH0NDE2E) (Active Moiety)
- INFLUENZA B VIRUS (UNII: 1314JZ2X6W)
- INFLUENZA B VIRUS (UNII: 1314JZ2X6W) (Active Moiety)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0)
- MYCOPLASMA PNEUMONIAE (UNII: JQE470FAD0) (Active Moiety)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K)
- HUMAN HERPESVIRUS 5 (UNII: 7COI029E6K) (Active Moiety)
- HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J)
- HUMAN PAPILLOMAVIRUS (UNII: 23CVL7WF4J) (Active Moiety)
- HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD)
- HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD) (Active Moiety)
- HUMAN COXSACKIEVIRUS B4 (UNII: FYF75V7FDY)
- HUMAN COXSACKIEVIRUS B4 (UNII: FYF75V7FDY) (Active Moiety)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2)
- STREPTOCOCCUS PNEUMONIAE (UNII: BT6U234YR2) (Active Moiety)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K)
- HUMAN BREAST TUMOR CELL (UNII: C62OO7VD9K) (Active Moiety)
Which are Biotox VI 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".